A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism
Patrícia B. S. Celestino-Soper(Baylor College of Medicine), Arthur L. Beaudet(Lunar and Planetary Institute), Bridget A. Fernandez(Memorial University of Newfoundland), Wendy Roberts(Holland Bloorview Kids Rehabilitation Hospital), Frédéric M. Vaz(Netherlands Metabolomics Centre), Emily L. Crawford(Vanderbilt University), Daniel H. Geschwind(University of California, Los Angeles), Timothy J. M. Moss(Melbourne Health), Kwanghyuk Lee, Diane Treadwell‐Deering(Texas Children's Hospital), Sara Violante(University of Lisbon), Joseph D. Buxbaum(Child Health and Development Institute), Elsa Delaby(Inserm), Ronald J. A. Wanders(Amsterdam University Medical Centers), Charlene Lo, Stephen W. Scherer(University of Toronto), Stephan Sanders(University of California, San Francisco), Roger E. Stevenson(Piedmont Technical College), Rui Luo(University of California, Los Angeles), Matthew E. Hurles(Wellcome Sanger Institute), Chad A. Shaw(Baylor College of Medicine), Bekim Sadiković(Western University), Jennifer R. German(Baylor College of Medicine), Anath C. Lionel(Radboud University Nijmegen), Catalina Betancur(Centre National de la Recherche Scientifique), Richard J. Schroer(Greenwood Genetic Center), Ni Huang(Shanghai Jiao Tong University), Suzanne M. Leal(Baylor College of Medicine), Kun Gao(University of California, Los Angeles), James S. Sutcliffe(Vanderbilt University), Robin P. Goin‐Kochel(Baylor College of Medicine), Péter Szatmári(University of Szeged), Guiqing Cai(King's College London), Marwan Shinawi(St. Louis Children's Hospital), Richard Person(GenVec), Edwin H. Cook(University of Chicago)
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