A De Novo Variant Identified in the PPP2R1A Gene in an Infant Induces Neurodevelopmental Abnormalities  

作　　者：Yanghui Zhang Haoxian Li Hua Wang Zhengjun Jia Hui Xi Xiao Mao 

机构地区：[1]National Health Commission Key Laboratory of Birth Defects Research,Prevention and Treatment,Hunan Provincial Maternal and Child Health Care Hospital,Changsha 410008,China

出　　处：《Neuroscience Bulletin》2020年第2期179-182,共4页神经科学通报（英文版）

基　　金：supported by the Science and Technology Department of Hunan Province,China(2017JJ3142).

摘　　要：Dear Editor,Neurodevelopmental disorders include a wide range of conditions such as epilepsy,intellectual disability,and autism spectrum disorder.These disorders commonly cooccur in patients,which suggests that they share a common etiology[1,2].Genetic advances resulting from sequencing techniques over the past few years have greatly expanded our understanding of neurodevelopmental disorders.

关 键 词：EPILEPSY expanded patients 

分 类 号：R748[医药卫生—神经病学与精神病学]