المؤلفون: Robert S. Wildin, Fred Ramsdell, Jane Peake, Ephrat Levy-Lahad, Olivier Goulet, Massimo Mazzella, Sean Proll, Franca Dagna Bricarelli, Geoffrey Byrne, Jean-Laurent Casanova, Mary E. Brunkow, L. Perroni, Mark McEuen, Francesca Faravelli, Mark Appleby, Neil R. M. Buist

المصدر: Nature Genetics. 27:18-20

مصطلحات موضوعية: medicine.medical_specialty, X Chromosome, Genetic Linkage, Protein-Losing Enteropathies, DNA Mutational Analysis, Molecular Sequence Data, Biology, Animal Diseases, Mice, Diabetes mellitus genetics, Neonatal diabetes mellitus, Diabetes mellitus, Internal medicine, Diabetes Mellitus, Genetics, medicine, Animals, Humans, Enteropathy, Amino Acid Sequence, Polyendocrinopathies, Autoimmune, Gene, X chromosome, Infant, Newborn, FOXP3, Forkhead Transcription Factors, Syndrome, IPEX syndrome, medicine.disease, Mice, Mutant Strains, DNA-Binding Proteins, Disease Models, Animal, Endocrinology, Mutation, Sequence Alignment

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1f5c6369a87c3719739ab2d18497ddf
https://doi.org/10.1038/83707