A common X-linked inborn error of carnitine biosynthesis may be a risk factor for non-dysmorphic autism

Patricia B. S. Celestino-Soper , Sara Violante , Emily L. Crawford , Rui Luo , Anath C. Lionel , Elsa Delaby , Guiqing Cai , Bekim Sadikovic , Kwanghyuk Lee , Charlene Lo , Kun Gao , Richard E. Person , Timothy J. Moss , Jennifer R. German , Ni Huang , Marwan Shinawi , Diane Treadwell-Deering , Peter Szatmari , Wendy Roberts , Bridget Fernandez , Richard J. Schroer , Roger E. Stevenson , Joseph D. Buxbaum , Catalina Betancur (1) , Stephen W. Scherer , Stephan J. Sanders , Daniel Geschwind , James S. Sutcliffe , Matthew E. Hurles , Ronald J. A. Wanders , Chad A. Shaw , Suzanne M. Leal , Edwin H. Cook , Robin P. Goin-Kochel , Frederic M. Vaz , Arthur L. Beaudet

1 NPS-01 - Génétique de l'autisme = Genetics of Autism

no abstract

Domaines: Neurosciences [q-bio.NC]

Patricia B. S. Celestino-Soper, Sara Violante, Emily L. Crawford, Rui Luo, Anath C. Lionel, et al.. A common X-linked inborn error of carnitine biosynthesis may be a risk factor for non-dysmorphic autism. 35th Annual Meeting of the Society-for-Inherited-Metabolic-Disorders (SIMD), Mar 2012, Charlotte, United States. pp.308-309. ⟨hal-01541312⟩