Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort.
Guo H, Peng Y, Hu Z, Li Y, Xun G, Ou J, Sun L, Xiong Z, Liu Y, Wang T, Chen J, Xia L, Bai T, Shen Y, Tian Q, Hu Y, Shen L, Zhao R, Zhang X, Zhang F, Zhao J, Zou X, Xia K.
Guo H, et al.
Sci Rep. 2017 Mar 10;7:44155. doi: 10.1038/srep44155.
Sci Rep. 2017.
PMID: 28281572
Free PMC article.
Clinical Trial.
The de novo 15q11-13 duplication was more prevalent in this Chinese population than in those with European ancestry. Several genes, including GRAMD2 and STAM, were implicated as novel ASD risk genes when integrating whole-genome CNVs and whole-exome sequencing data. ...
The de novo 15q11-13 duplication was more prevalent in this Chinese population than in those with European ancestry. Several genes, includin …