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Biological Effects of COMT Haplotypes and Psychosis Risk in 22q11.2 Deletion Syndrome
Authors:Doron Gothelf  Amanda J. Law  Amos Frisch  Jingshan Chen  Omer Zarchi  Elena Michaelovsky  Renee Ren-Patterson  Barbara K. Lipska  Miri Carmel  Bhaskar Kolachana  Abraham Weizman  Daniel R. Weinberger
Affiliation:1. Behavioral Neurogenetics Center, Edmond and Lily Safra Children’s Hospital, Sheba Medical Center, Tel Hashomer, Israel;2. Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel;3. Departments of Psychiatry and Cell and Developmental Biology, School of Medicine, University of Colorado, Aurora, Colorado;4. Clinical Brain Disorders Branch, Intramural Research Program, National Institute of Mental Health, National Institutes of Health, Bethesda, Maryland;5. The Felsenstein Medical Research Center, Petah Tiqwa, Israel;6. Lieber Institute for Brain Development, Johns Hopkins University Medical Campus;g Departments of Psychiatry, Neurology, and Neuroscience and the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland
Abstract:
Keywords:COMT   DiGeorge   gene expression   haplotype   psychosis   velocardiofacial syndrome
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