Electrophysiological Phenotypes of MeCP2 A140V Mutant Mouse Model

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 bra...

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Detalhes bibliográficos
Publicado no:CNS Neurosci Ther
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2014
Assuntos:
Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6493136/
https://ncbi.nlm.nih.gov/pubmed/24750778
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cns.12229
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