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Separate Respiratory Phenotypes in Methyl-CpG-Binding Protein 2 (Mecp2) Deficient Mice

Rett syndrome (RTT) is a neurodevelopmental disorder caused by mutations in the X-linked gene methyl-CpG-binding protein 2 (MECP2) that encodes a DNA binding protein involved in gene silencing. Selective deletion of Mecp2 in post-mitotic neurons in mice results in a Rettlike phenotype characterized...

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Detalhes bibliográficos
Main Authors: BISSONNETTE, JOHN M., KNOPP, SHARON J.
Formato: Artigo
Idioma:Inglês
Publicado em: 2006
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1473964/
https://ncbi.nlm.nih.gov/pubmed/16549521
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1203/01.pdr.0000203157.31924.4a
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