High proportion of 22q13 deletions and SHANK3 mutations in Chinese patients with intellectual disability.

High proportion of 22q13 deletions and SHANK3 mutations in Chinese patients with intellectual disability.

Intellectual disability (ID) is a heterogeneous disorder caused by chromosomal abnormalities, monogenic factors and environmental factors. 22q13 deletion syndrome is a genetic disorder characterized by severe ID. Although the frequency of 22q13 deletions in ID is unclear, it is believed to be largel...

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Bibliographic Details
Main Authors: Xiaohong Gong, Yu-Wu Jiang, Xin Zhang, Yu An, Jun Zhang, Ye Wu, Jingmin Wang, Yangfei Sun, Yanyan Liu, Xuewu Gao, Yiping Shen, Xiru Wu, Zilong Qiu, Li Jin, Bai-Lin Wu, Hongyan Wang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3324537?pdf=render

Internet

http://europepmc.org/articles/PMC3324537?pdf=render

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