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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Detalles Bibliográficos
Autores principales: Gong, Xiaohong, Jiang, Yu-wu, Zhang, Xin, An, Yu, Zhang, Jun, Wu, Ye, Wang, Jingmin, Sun, Yangfei, Liu, Yanyan, Gao, Xuewu, Shen, Yiping, Wu, Xiru, Qiu, Zilong, Jin, Li, Wu, Bai-Lin, Wang, Hongyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3324537/
https://www.ncbi.nlm.nih.gov/pubmed/22509352
http://dx.doi.org/10.1371/journal.pone.0034739

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3324537/
https://www.ncbi.nlm.nih.gov/pubmed/22509352
http://dx.doi.org/10.1371/journal.pone.0034739

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