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1
المؤلفون: Kelly D. Foote, Robert L. Nussbaum, Cynthia Crews, Coro Paisán-Ruiz, Sharon Reimsnider, Michael S. Okun, Grisel Lopez, Hubert H. Fernandez, E. Whitney Evans, Katrina Gwinn-Hardy, Aideen M. McInerney-Leo, Anthony Crawley, Angela Britton, Andrew B. Singleton, Roniel Malkani, Janel O. Johnson, Ronald J. Mandel, Shushant Jain
المصدر: Neurodegenerative Diseases. 4:386-391
مصطلحات موضوعية: Genetics, Mutation, Parkinson's disease, Parkinsonism, Biology, medicine.disease_cause, medicine.disease, LRRK2, nervous system diseases, Exon, Neurology, Cohort, medicine, Missense mutation, Neurology (clinical), Family history
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2
المؤلفون: Janel, Johnson, Coro, Paisán-Ruíz, Grisel, Lopez, Cynthia, Crews, Angela, Britton, Roniel, Malkani, E Whitney, Evans, Aideen, McInerney-Leo, Shushant, Jain, Robert L, Nussbaum, Kelly D, Foote, Ronald J, Mandel, Anthony, Crawley, Sharon, Reimsnider, Hubert H, Fernandez, Michael S, Okun, Katrina, Gwinn-Hardy, Andrew B, Singleton
المصدر: Neuro-degenerative diseases. 4(5)
مصطلحات موضوعية: Adult, Aged, 80 and over, Brain Chemistry, Genetic Markers, Male, Adolescent, Base Sequence, DNA Mutational Analysis, Molecular Sequence Data, Mutation, Missense, Parkinson Disease, Middle Aged, Protein Serine-Threonine Kinases, Leucine-Rich Repeat Serine-Threonine Protein Kinase-2, Cohort Studies, Alternative Splicing, Amino Acid Substitution, Mutation, North America, Humans, Genetic Predisposition to Disease, Amino Acid Sequence, Genetic Testing, RNA Splice Sites, Aged