Novel PAK3 gene missense variant associated with two Chinese siblings with intellectual disability: a case report | BMC Medical Genetics | Full Text

Novel PAK3 gene missense variant associated with two Chinese siblings with intellectual disability: a case report | BMC Medical Genetics | Full Text

Novel PAK3 gene missense variant associated with two Chinese siblings with intellectual disability: a case report

Intellectual disability (ID) constitutes the most common group of neurodevelopmental disorders. Exome sequencing has enabled the discovery of genetic mutations responsible for a wide range of ID disorders.

Authors:Yanyan Qian, Bingbing Wu, Yulan Lu, Wenhao Zhou, Sujuan Wang and Huijun Wang

Citation:BMC Medical Genetics 2020 21:31

Content type:Case report

Published on: 12 February 2020

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