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QT(c) interval and ventricular action potential prolongation in the Mecp2 ( Null/+) murine model of Rett syndrome
Rett Syndrome (RTT) is a congenital, X‐chromosome‐linked developmental disorder characterized by developmental delay, dysautonomia, and breathing irregularities. RTT is also associated with sudden death and QT intervals are prolonged in some RTT patients. Most individuals with RTT have mutations in...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9535259/ https://www.ncbi.nlm.nih.gov/pubmed/36200140 http://dx.doi.org/10.14814/phy2.15437 |