Associated Papers
Rare UNC13B variations and risk of schizophrenia: Whole-exome sequencing in a multiplex family and follow-up resequencing and a case-control study.
Egawa J et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2016
Mutations of ANK3 identified by exome sequencing are associated with autism susceptibility.
Bi C et al.
Human Mutation, 2012
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