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...

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Detalles Bibliográficos
Autores principales: Cheng, Hongwei, Charles, Ian, James, Andrew F., Abdala, Ana P., Hancox, Jules C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Original Articles
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

Internet

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

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