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1Academic Journal
المؤلفون: Michael S. L. Ching, Yiping Shen, Wen-hann Tan, Shafali S. Jeste, Eric M. Morrow, Xiaoli Chen, Nahit M. Mukaddes, Seung-yun Yoo, Ellen Hanson, Rachel Hundley, Christina Austin, Ronald E. Becker, Gerard T. Berry, Katherine Driscoll, Elizabeth C. Engle, Ra Friedman, James F. Gusella, Fuki M. Hisama, Mira B. Irons, Tina Lafiosca, Elaine Leclair, David T. Miller, Michael Neessen, Jonathan D. Picker, Cynthia M. Rooney, Dean P. Sarco, Joan M. Stoler, Christopher A. Walsh, Robert R. Wolff, Ting Zhang, Ramzi H. Nasir, Bai-lin Wu, Genotype Phenotype, Study Group, Includes Omar S. Khwaja, Annapurna Poduri, Mustafa Sahin
المساهمون: The Pennsylvania State University CiteSeerX Archives
المصدر: http://www.walshlab.org/pdf/ChingDeletionsofNRXN1developmentaldisordersAmJMedGenetB2010.pdf.
وصف الملف: application/pdf
Relation: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.599.7752; http://www.walshlab.org/pdf/ChingDeletionsofNRXN1developmentaldisordersAmJMedGenetB2010.pdf
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2Academic Journal
المؤلفون: Eric M. Morrow, Seung-yun Yoo, Steven W. Flavell, Tae-kyung Kim, Robert M. Joseph, Rachel Greenblatt, Danielle Gleason, Julia A. Ertelt, Kira A. Apse, Adria Bodell, Jennifer N. Partlow, Brenda Barry, Hui Yao, Kyriacos Markianos, Russell J. Ferl, Michael E. Greenberg, Christopher A. Walsh
المساهمون: The Pennsylvania State University CiteSeerX Archives
وصف الملف: application/pdf
Relation: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.205.6567; http://www.childrenshospital.org/bcrp/AutismScience_Walsh2009.pdf
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3
المؤلفون: Matthew Schwede, R. Sean Hill, Anna Rajab, Ramzi Nasir, Muna Al-Saffar, Eric M. Morrow, Michael Schmidt, Sofia B. Lizarraga, Shailender Nagpal, Anh Thu N. Lam, Shawn M. Davidson, Sasmita Mishra, Mirrat Gul Butt, Haroon Rashid Chaudhry, Malak Ei-Quessny, Afzal Javed, Ralph J. DeBerardinis, Syed Imran Murtaza, Tojo Nakayama, Seung Yun Yoo, Ozan Baytas, Ganeshwaran H. Mochida, Chendong Yang, David E. Housman, A. James Barkovich, Jennifer N. Partlow, Saima Niaz, Dylan J. Vaughan, Qing Ouyang
المصدر: Proceedings of the National Academy of Sciences. 113
مصطلحات موضوعية: 0301 basic medicine, Citric Acid Cycle, Mutation, Missense, Biology, Mitochondrion, Neuroprotection, Mice, 03 medical and health sciences, 0302 clinical medicine, Pyruvic Acid, Animals, Humans, Missense mutation, Amino Acid Sequence, Transaminases, Loss function, Alanine, Genetics, Multidisciplinary, Homozygote, Glutamate receptor, Brain, Mitochondria, Citric acid cycle, Phenotype, 030104 developmental biology, PNAS Plus, Alanine transaminase, biology.protein, Ketoglutaric Acids, Nervous System Diseases, 030217 neurology & neurosurgery
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4
المؤلفون: Brenda E. Barry, Tae Kyung Kim, Kyriacos Markianos, Robert Sean Hill, Jennifer N. Partlow, Russell J. Ferland, Hui Yao, Samira Al-Saad, Danielle Gleason, Rachel Greenblatt, Julia A. Ertelt, Robert M. Joseph, Kira Apse, Adria Bodell, Christopher A. Walsh, Steven W. Flavell, Yingxi Lin, Michael E. Greenberg, Janice Ware, Generoso G. Gascon, Soher Balkhy, Nahit Motavalli Mukaddes, Seung-Yun Yoo, Asif Hashmi, Eric M. Morrow
المصدر: Science. 321:218-223
مصطلحات موضوعية: Male, Sodium-Hydrogen Exchangers, Gene Dosage, Formins, Protocadherin, Genes, Recessive, Locus (genetics), Biology, Polymorphism, Single Nucleotide, Gene dosage, Article, Consanguinity, medicine, Animals, Humans, Genetic Predisposition to Disease, Autistic Disorder, Gene, Adaptor Proteins, Signal Transducing, Oligonucleotide Array Sequence Analysis, Neurons, Regulation of gene expression, Genetics, Multidisciplinary, Homozygote, Brain, Chromosome Mapping, Cadherins, medicine.disease, Disease gene identification, Protocadherins, Pedigree, Rats, Developmental disorder, Gene Expression Regulation, Mutation, Autism, Female, Lod Score, Gene Deletion, Transcription Factors
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5
المؤلفون: Salem Kathiri, Riaz Ahmed, Christopher A. Walsh, Ganeshwaran H. Mochida, Aiman Abdulgalil, Seung-Yun Yoo, Anna Rajab, Adria Bodell, A. James Barkovich
المصدر: American Journal of Medical Genetics Part A. :1504-1510
مصطلحات موضوعية: Male, Microcephaly, Pediatrics, medicine.medical_specialty, Adolescent, Oman, Genes, Recessive, Neurological disorder, Hyperreflexia, Article, Cerebral palsy, Consanguinity, Dysarthria, Spastic cerebral palsy, Intellectual Disability, Spastic diplegia, Genetics, medicine, Humans, Child, Genetics (clinical), business.industry, Cerebral Palsy, Diplegia, Syndrome, medicine.disease, Magnetic Resonance Imaging, Pedigree, Phenotype, Female, medicine.symptom, business
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6
المؤلفون: Christopher A. Walsh, Judy S. Liu, Joseph C. Corbo, Thomas A.S. Deuel, Lucy B. Rorke-Adams, Seung-Yun Yoo
المصدر: Neuron. 49(1):41-53
مصطلحات موضوعية: 0303 health sciences, General Neuroscience, Neuroscience(all), Mutant, Anterior commissure, Biology, Hippocampal formation, Synaptic vesicle, Doublecortin, Vesicular transport protein, 03 medical and health sciences, 0302 clinical medicine, nervous system, Microtubule, Axoplasmic transport, biology.protein, Neuroscience, 030217 neurology & neurosurgery, 030304 developmental biology
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7
المؤلفون: Dawna L. Armstrong, Richard Atkinson, Samuel M. Wu, J. David Sweatt, Shiming Chen, Bisong Xu, Huda Y. Zoghbi, Edwin J. Weeber, Mark E. Pennesi, Seung-Yun Yoo
المصدر: Neuron. 37:383-401
مصطلحات موضوعية: Male, Ataxin 7, Ataxia, Neuroscience(all), Long-Term Potentiation, Mutant, Gene Expression, Mice, Transgenic, Nerve Tissue Proteins, Hippocampus, Mice, Downregulation and upregulation, Retinal Rod Photoreceptor Cells, Cerebellum, medicine, Animals, Humans, Spinocerebellar Ataxias, Gene, Ataxin-7, Homeodomain Proteins, Neurons, Neuronal Plasticity, biology, General Neuroscience, Long-term potentiation, medicine.disease, Cell biology, Glutamine, Disease Models, Animal, Phenotype, Solubility, Retinal Cone Photoreceptor Cells, Trans-Activators, Spinocerebellar ataxia, biology.protein, Female, medicine.symptom, Neuroscience, Retinitis Pigmentosa
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8
المؤلفون: Ramzi Nasir, Jonathan Picker, Mira Irons, Ronald E. Becker, Tina Lafiosca, Christopher A. Walsh, Sandra L. Friedman, Christina A. Austin, Yiping Shen, Eric M. Morrow, Cynthia M. Rooney, Elaine LeClair, Dean Sarco, Nahit Motavalli Mukaddes, Michael Neessen, Elizabeth C. Engle, Wen-Hann Tan, Michael S L Ching, Fuki M. Hisama, Bai-Lin Wu, Katherine Driscoll, Ellen Hanson, Xiaoli Chen, Leonard Rappaport, Joan M. Stoler, Shafali S. Jeste, Seung Yun Yoo, Gerard T. Berry, Rachel J. Hundley, James F. Gusella, Ting Zhang, David T. Miller, Robert Wolff
المصدر: Ching, MSL; Shen, Y; Tan, WH; Jeste, SS; Morrow, EM; Chen, X; et al.(2010). Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 153(4), 937-947. doi: 10.1002/ajmg.b.31063. UCLA: Retrieved from: http://www.escholarship.org/uc/item/6zj2639n
American Journal of Medical Geneticsمصطلحات موضوعية: Male, NRXN1 exonic deletions, Developmental Disabilities, CNV, Single-nucleotide polymorphism, Array CGH, Biology, NRXN1 (neurexin-1), 03 medical and health sciences, Cellular and Molecular Neuroscience, 0302 clinical medicine, Intellectual Disability, Genotype, medicine, array CGH, Humans, Heritability of autism, developmental disorders, Language Development Disorders, Allele, Autistic Disorder, Child, Genetics (clinical), Research Articles, 030304 developmental biology, Sequence Deletion, Genetics, 0303 health sciences, Comparative Genomic Hybridization, Developmental disorders, medicine.disease, Disease gene identification, Hypotonia, 3. Good health, Psychiatry and Mental health, Phenotype, Child Development Disorders, Pervasive, Mutation, Schizophrenia, Autism, Female, medicine.symptom, 030217 neurology & neurosurgery, Comparative genomic hybridization
وصف الملف: application/pdf
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9
المؤلفون: Zak Kohane, Jeremy Goldberg, Carine Mantoulan, Shaun Purcell, Jessica Brian, Magdalena Laskawiec, Christopher A. Walsh, Irma Moilanen, Ridha Joober, Peter Szatmari, Olena Korvatska, Kerim Munir, James F. Gusella, Rudolph E. Tanzi, David L. Pauls, Generoso G. Gascon, Christine Stevens, Linda Lotspeich, John I. Nurnberger, Ramzi Nazir, Jonathan Green, Brian L. Yaspan, Marion Leboyer, Ann P. Thompson, Shun-Chiao Chang, Carolyn Bridgemohan, Louise Gallagher, Jeff Munson, Michael Gill, Guiqing Cai, Fritz Poustka, Regina Regan, Aislyn Cangialose, Gerard D. Schellenberg, Christopher J. McDougle, Christina Corsello, Wendy Roberts, Thomas H. Wassink, Majid Ghadami, Ellen M. Hanson, Benjamin M. Neale, Stacey Gabriel, Lonnie Zwaigenbaum, John Tsiantis, Hanna Ebeling, Sabine M. Klauck, Elaine LeClair, Bernie Devlin, Steven A. McCarroll, Ashley O'Connor, Andrew Pickles, Emily L. Crawford, Katja Jussila, Helen McConachie, Christopher Gillberg, Brenda E. Barry, Lou Kunkel, Seung Yun Yoo, Jennifer N. Partlow, Stephanie Brewster O'Neil, Ingrid A. Holm, Judith Miller, Guy A. Rouleau, Val C. Sheffield, Catherine Lord, Judith S. Palfrey, Ellen M. Wijsman, Astrid M. Vicente, Azam Hosseinipour, Ronald E. Becker, James S. Sutcliffe, Fred R. Volkmar, Marja Leena Mattila, Katerina Papanikolaou, Jennifer Reichert, Edwin H. Cook, Pamela Sklar, Elena Maestrini, Hilary Coon, Sek Won Kong, Stephen A. Haddad, Todd Green, Gillian Baird, Andrew Kirby, Patrick Bolton, Robert Sean Hill, Eric M. Morrow, Tom Berney, Jonathan L. Haines, Maryam Valujerdi, Casey Gates, David J. Posey, Karola Rehnström, Alistair T. Pagnamenta, Christine M. Freitag, Eric Fombonne, Janice Ware, Christian R. Marshall, Janine A. Lamb, Lauren A. Weiss, Agatino Battaglia, Nancy J. Minshew, Roksana Sasanfar, Elizabeth Baroni, Maretha de Jonge, Lennart von Wendt, Gina Hilton, Dalila Pinto, Nahit Motavalli Mukaddes, Ala Tolouei, Catalina Betancur, Michael Rutter, Tram Tran, Eftichia Duketis, Laurent Mottron, Margaret A. Pericak-Vance, Kristen West, Joachim Hallmayer, Kirsty Wing, Kerstin Wittemeyer, Rachel J. Hundley, Herman van Engeland, Judith Conroy, Mark J. Daly, Asif Hashmi, Michael L. Cuccaro, Geraldine Dawson, Sanna Kuusikko, Richard Anney, Anthony P. Monaco, Brian Winkloski, Samira Al-Saad, Dan E. Arking, Veronica J. Vieland, Stephen W. Scherer, Soher Balkhy, Kara Andresen, Rebecca L. Tomlinson, Joseph D. Buxbaum, Aravinda Chakravarti, Xiao-Qing Liu, Lindsay Jackson, Jaakko Ignatius, Catarina Correia, Leonard Rappaport, Heather Peters, Julie Gauthier, John R. Gilbert, Jeremy R. Parr, Carrie Sougnez, Katherine E. Tansey, Bennett L. Leventha, Annemarie Poustka, Daniel H. Geschwind, Annette Estes, Leena Peltonen, Maryam Rostami, Jeff Salt, David Altshuler, Simon Wallace, Susan E. Bryson, William M. Mahoney, Katy Renshaw, Robert M. Joseph, Lisa H. Albers, Inês Cabrito, Sean Ennis, Vanessa Hus, Guiomar Oliveira, Ann Le Couteur, Joseph Piven, Sandra L. Friedman, Penny Farrar, Joshua M. Korn, Sven Bölte, Camille W. Brune, Esau Simmons, Susan L. Santangelo, Andrew D. Paterson, Rita M. Cantor, Andrew B. West, Finny G Kuruvilla, Tiago R. Magalhaes, Andrew Green, Alison Schonwald, Stephen J. Guter, Anthony J. Bailey, Bernadette Rogé, William M. McMahon
المساهمون: Massachusetts General Hospital [Boston], Harvard Medical School [Boston] (HMS), Broad Institute of MIT and Harvard (BROAD INSTITUTE), Harvard Medical School [Boston] (HMS)-Massachusetts Institute of Technology (MIT)-Massachusetts General Hospital [Boston], Johns Hopkins University (JHU), Helsingin yliopisto = Helsingfors universitet = University of Helsinki, Génétique de l'autisme = Genetics of Autism (NPS-01), Neuroscience Paris Seine (NPS), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut de Biologie Paris Seine (IBPS), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut de Biologie Paris Seine (IBPS), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Betancur, Catalina, University of Helsinki, Neurosciences Paris Seine (NPS), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut de Biologie Paris Seine (IBPS), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut de Biologie Paris Seine (IBPS), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS), WEISS LA, ARKING DE, GENE DISCOVERY PROJECT OF JOHNS HOPKINS & THE AUTISM CONSORTIUM, DALY MJ, CHAKRAVARTI A, BRUNE CW, WEST K, O'CONNOR A, HILTON G, TOMLINSON RL, WEST AB, COOK EH JR, CHAKRAVARTI A, WEISS LA, GREEN T, CHANG SC, GABRIEL S, GATES C, HANSON EM, KIRBY A, KORN J, KURUVILLA F, MCCARROLL S, MORROW EM, NEALE B, PURCELL S, SASANFAR R, SOUGNEZ C, STEVENS C, ALTSHULER D, GUSELLA J, SANTANGELO SL, SKLAR P, TANZI R, DALY MJ, ANNEY R, BAILEY AJ, BAIRD G, BATTAGLIA A, BERNEY T, BETANCUR C, BÖLTE S, BOLTON PF, BRIAN J, BRYSON SE, BUXBAUM JD, CABRITO I, CAI G, CANTOR RM, COOK EH JR, COON H, CONROY J, CORREIA C, CORSELLO C, CRAWFORD EL, CUCCARO ML, DAWSON G, DE JONGE M, DEVLIN B, DUKETIS E, ENNIS S, ESTES A, FARRAR P, FOMBONNE E, FREITAG CM, GALLAGHER L, GESCHWIND DH, GILBERT J, GILL M, GILLBERG C, GOLDBERG J, GREEN A, GREEN J, GUTER SJ, HAINES JL, HALLMAYER JF, HUS V, KLAUCK SM, KORVATSKA O, LAMB JA, LASKAWIEC M, LEBOYER M, COUTEUR AL, LEVENTHAL BL, LIU XQ, LORD C, LOTSPEICH LJ, MAESTRINI E, MAGALHAES T, MAHONEY W, MANTOULAN C, MCCONACHIE H, MCDOUGLE CJ, MCMAHON WM, MARSHALL CR, MILLER J, MINSHEW NJ, MONACO AP, MUNSON J, NURNBERGER JI JR, OLIVEIRA G, PAGNAMENTA A, PAPANIKOLAOU K, PARR JR, PATERSON AD, PERICAK-VANCE MA, PICKLES A, PINTO D, PIVEN J, POSEY DJ, POUSTKA A, POUSTKA F, REGAN R, REICHERT J, RENSHAW K, ROBERTS W, ROGE B, RUTTER ML, SALT J, SCHELLENBERG GD, SCHERER SW, SHEFFIELD V, SUTCLIFFE JS, SZATMARI P, TANSEY K, THOMPSON AP, TSIANTIS J, VAN ENGELAND H, VICENTE AM, VIELAND VJ, VOLKMAR F, WALLACE S, WASSINK TH, WIJSMAN EM, WING K, WITTEMEYER K, YASPAN BL, ZWAIGENBAUM L, MORROW EM, YOO SY, HILL RS, MUKADDES NM, BALKHY S, GASCON G, AL-SAAD S, HASHMI A, WARE J, JOSEPH RM, LECLAIR E, PARTLOW JN, BARRY B, WALSH CA, PAULS D, MOILANEN I, EBELING H, MATTILA ML, KUUSIKKO S, JUSSILA K, IGNATIUS J, SASANFAR R, TOLOUEI A, GHADAMI M, ROSTAMI M, HOSSEINIPOUR A, VALUJERDI M, SANTANGELO SL, ANDRESEN K, WINKLOSKI B, HADDAD S, KUNKEL L, KOHANE Z, TRAN T, KONG SW, O'NEIL SB, HANSON EM, HUNDLEY R, HOLM I, PETERS H, BARONI E, CANGIALOSE A, JACKSON L, ALBERS L, BECKER R, BRIDGEMOHAN C, FRIEDMAN S, MUNIR K, NAZIR R, PALFREY J, SCHONWALD A, SIMMONS E, RAPPAPORT LA, GAUTHIER J, MOTTRON L, JOOBER R, FOMBONNE E, ROULEAU G, REHNSTROM K, VON WENDT L, PELTONEN L.
المصدر: Nature
Nature, 2009, 461 (7265), pp.802-808. ⟨10.1038/nature08490⟩
Nature, Nature Publishing Group, 2009, 461 (7265), pp.802-808. ⟨10.1038/nature08490⟩مصطلحات موضوعية: Perturbação Autística, Internationality, Genetic Linkage, Genome-wide association study, MESH: Semaphorins, Semaphorins, [SDV.GEN] Life Sciences [q-bio]/Genetics, 0302 clinical medicine, Neurodevelopmental disorder, Heritability of autism, MESH: Nerve Tissue Proteins, Association mapping, Genetics, 0303 health sciences, Multidisciplinary, MESH: Polymorphism, Single Nucleotide, MESH: Genetic Predisposition to Disease, Brain, Chromosome Mapping, Chromosomes, Human, Pair 5, MESH: Membrane Proteins, MESH: Chromosomes, Human, Pair 5, MESH: Autistic Disorder, MESH: Genetic Linkage, Single-nucleotide polymorphism, Nerve Tissue Proteins, Biology, Polymorphism, Single Nucleotide, Article, 03 medical and health sciences, MESH: Brain, Genetic linkage, medicine, Humans, Genetic Predisposition to Disease, Autistic Disorder, MESH: Sample Size, 030304 developmental biology, Genetic association, [SDV.GEN]Life Sciences [q-bio]/Genetics, MESH: Humans, Membrane Proteins, medicine.disease, Sample Size, Perturbações do Desenvolvimento Infantil e Saúde Mental, MESH: Genome-Wide Association Study, MESH: Internationality, Autism, MESH: Chromosome Mapping, Predisposição Genética para Doença, 030217 neurology & neurosurgery, Genome-Wide Association Study
وصف الملف: STAMPA
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10
المؤلفون: Aaron B. Bowman, Nico P. Dantuma, Seung-Yun Yoo, Huda Y. Zoghbi
المصدر: Human molecular genetics. 14(5)
مصطلحات موضوعية: Genetically modified mouse, Proteasome Endopeptidase Complex, Intranuclear Inclusion Bodies, Nerve Tissue Proteins, Neuropathology, Green fluorescent protein, Mice, Huntington's disease, Ubiquitin, Genes, Reporter, Genetics, medicine, Animals, Spinocerebellar Ataxias, Photoreceptor Cells, RNA, Messenger, Molecular Biology, Genetics (clinical), Ataxin-7, Neurons, biology, General Medicine, medicine.disease, Cell biology, Disease Models, Animal, medicine.anatomical_structure, Biochemistry, Proteasome, Spinocerebellar ataxia, biology.protein, Neuron, Peptides
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11Academic Journal
المؤلفون: Thomas A. S. Deuel, Judy S. Liu, Joseph C. Corbo, Seung-yun Yoo, Lucy B. Rorke-adams, Christopher A. Walsh
المساهمون: The Pennsylvania State University CiteSeerX Archives
وصف الملف: application/pdf
Relation: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.597.1696; http://www.walshlab.org/pdf/deuel.pdf
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12Academic Journal
المؤلفون: Qing Ouyang, Tojo Nakayama, Baytas, Ozan, Davidson, Shawn M., Chendong Yang, Schmidt, Michael, Lizarraga, Sofia B., Mishra, Sasmita, EI-Quessny, Malak, Niaz, Saima, Butt, Mirrat Gul, Murtaza, Syed Imran, Javed, Afzal, Chaudhry, Haroon Rashid, Vaughan, Dylan J., Hill, R. Sean, Partlow, Jennifer N., Seung-Yun Yoo, Lam, Anh-Thu N., Nasir, Ramzi
المصدر: Proceedings of the National Academy of Sciences of the United States of America; 9/20/2016, Vol. 113 Issue 38, pE5598-E5607, 10p
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