Molecular stratification of arrhythmogenic mechanisms in the Andersen Tawil syndrome

Andersen-Tawil syndrome (ATS) is a rare inheritable disease associated with loss-of-function mutations in KCNJ2, the gene coding the strong inward rectifier potassium channel Kir2.1, which forms an essential membrane protein controlling cardiac excitability. ATS is usually marked by a triad of perio...

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Detalles Bibliográficos
Autores principales: Moreno-Manuel, Ana Isabel, Gutiérrez, Lilian K, Vera-Pedrosa, María Linarejos, Cruz, Francisco Miguel, Bermúdez-Jiménez, Francisco José, Martínez-Carrascoso, Isabel, Sánchez-Pérez, Patricia, Macías, Álvaro, Jalife, José
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10153646/
https://www.ncbi.nlm.nih.gov/pubmed/35892314
http://dx.doi.org/10.1093/cvr/cvac118

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10153646/
https://www.ncbi.nlm.nih.gov/pubmed/35892314
http://dx.doi.org/10.1093/cvr/cvac118

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