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Breathing dysfunction in Rett syndrome: Understanding epigenetic regulation of the respiratory network

Severely arrhythmic breathing is a hallmark of Rett syndrome (RTT) and profoundly affects quality of life for patients and their families. The last decade has seen the identification of the disease-causing gene, methyl-CpG-binding protein 2 (Mecp2) and the development of mouse models that phenocopy...

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Detalhes bibliográficos
Main Authors: Ogier, Michael, Katz, David M.
Formato: Artigo
Idioma:Inglês
Publicado em: 2008
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2664709/
https://ncbi.nlm.nih.gov/pubmed/18534925
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.resp.2008.04.005
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