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Defects in brainstem neurons associated with breathing and motor function in the Mecp2(R168X/Y) mouse model of Rett syndrome
Rett Syndrome (RTT) is an X-linked neurodevelopmental disorder caused mostly by disruption of the MECP2 gene. Among several RTT-like mouse models, one of them is a strain of mice that carries an R168X point mutation in Mecp2 and resembles one of the most common RTT-causing mutations in humans. Altho...
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| Publicado no: | Am J Physiol Cell Physiol |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Physiological Society
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5206293/ https://ncbi.nlm.nih.gov/pubmed/27653984 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajpcell.00132.2016 |
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