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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Detalles Bibliográficos
Autores principales: Zhou, Bingbo, Zhang, Chuan, Zheng, Lei, Wang, Zhiqiang, Chen, Xue, Feng, Xuan, Zhang, Qinghua, Hao, Shengju, Wei, Liwan, Gu, Weiyue, Hui, Ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8655903/
https://www.ncbi.nlm.nih.gov/pubmed/34899870
http://dx.doi.org/10.3389/fgene.2021.794766

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8655903/
https://www.ncbi.nlm.nih.gov/pubmed/34899870
http://dx.doi.org/10.3389/fgene.2021.794766

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