Case Report: A Novel De Novo Missense Mutation of the GRIA2 Gene in a Chinese Case of Neurodevelopmental Disorder With Language Impairment

Case Report: A Novel De Novo Missense Mutation of the GRIA2 Gene in a Chinese Case of Neurodevelopmental Disorder With Language Impairment

Introduction: Neurodevelopmental disorders with language impairment and behavioral abnormalities (NEDLIB) are a disease caused by heterozygous variants in the glutamate ionotropic receptor AMPA type subunit 2 (GRIA2) gene, which manifest as impaired mental development or developmental delay, behavio...

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Bibliographic Details
Main Authors: Bingbo Zhou, Chuan Zhang, Lei Zheng, Zhiqiang Wang, Xue Chen, Xuan Feng, Qinghua Zhang, Shengju Hao, Liwan Wei, Weiyue Gu, Ling Hui
Format: article
Language:EN
Published: Frontiers Media S.A. 2021
Subjects:
GRIA2 gene
case report
neurodevelopmental disorder
language impairment
behavioral abnormalities
Genetics
QH426-470
Online Access:https://doaj.org/article/afb0017971ea4aa8a75e9fa9af8fc0b1
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https://doaj.org/article/afb0017971ea4aa8a75e9fa9af8fc0b1

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