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Methyl-CpG binding-protein 2 function in cholinergic neurons mediates cardiac arrhythmogenesis
Sudden unexpected death occurs in one quarter of deaths in Rett Syndrome (RTT), a neurodevelopmental disorder caused by mutations in Methyl-CpG-binding protein 2 (MECP2). People with RTT show a variety of autonomic nervous system (ANS) abnormalities and mouse models show similar problems including Q...
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| Publicado no: | Hum Mol Genet |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6078594/ https://ncbi.nlm.nih.gov/pubmed/28159985 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddw326 |
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