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Article

Electrophysiological phenotypes of MeCP2 A140V mutant mouse model.

CNS neuroscience & therapeutics - 1 May 2014

Ma Lu-Yao, Wu Chen, Jin Yu, Gao Ming, Li Guo-Hui, Turner Dharshaun, Shen Jian-Xin, Zhang Shi-Jiang, Narayanan Vinodh, Jentarra Garilyn, Wu Jie

Abstract excerpt

AIMS: MeCP2 gene mutations are associated with Rett syndrome and X-linked mental retardation (XLMR), diseases characterized by abnormal brain development and function. Recently, we created a novel MeCP2 A140V mutation mouse model that exhibited abnormalities of cell packing density and dendritic branching consistent with that seen in Rett syndrome patients as well as other MeCP2 mutant mouse models. Therefore, we...

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Identifiers

PMID: 24750778
DOI: 10.1111/cns.12229
PMCID: PMC6493136

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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