Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders

Autor: 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

Publikováno v: 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 Genetics

Research has implicated mutations in the gene for neurexin-1 (NRXN1) in a variety of conditions including autism, schizophrenia, and nicotine dependence. To our knowledge, there have been no published reports describing the breadth of the phenotype a

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http://www.escholarship.org/uc/item/6zj2639n