Three intellectual disability-associated de novo mutations in MECP2 identified by trio-WES analysis

To date, at least 746 genes have been identified to cause intellectual disability (ID). Among them, mutations in the Methyl CpG binding protein 2 (MECP2) gene are the leading cause of Rett syndrome and associated...

Source: BMC Medical Genetics - May 11, 2020 Category: Genetics & Stem Cells Authors: Yi Gu, Bingwu Xiang, Lina Zhu, Xiuwei Ma, Xiang Chen and Tao Cai Tags: Research article Source Type: research