Article
Association of IMMP2L deletions with autism spectrum disorder: A trio family study and meta-analysis.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics - 1 Jan 2018
Zhang Yanqing, Liu Yi, Zarrei Mehdi, Tong Winnie, Dong Rui, Wang Ying, Zhang Haiyan, Yang Xiaomeng, MacDonald Jeffrey R, Uddin Mohammed, Scherer Stephen W, Gai Zhongtao
Abstract excerpt
IMMP2L, the gene encoding the inner mitochondrial membrane peptidase subunit 2-like protein, has been reported as a candidate gene for Tourette syndrome, autism spectrum disorder (ASD) and additional neurodevelopmental disorders. Here we genotyped 100 trio families with an index proband with autism spectrum disorder in Han Chinese population and found three cases with rare exonic IMMP2L deletions. We have...
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