Case Report: Loss-of-Function ABCC9 Genetic Variant Associated With Ventricular Fibrillation

Genetic variants in the ABCC9 gene, encoding the SUR2 auxiliary subunit from K(ATP) channels, were previously linked with various inherited diseases. This wide range of congenital disorders includes multisystem and cardiovascular pathologies. The gain-of-function mutations result in Cantu syndrome,...

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Detalles Bibliográficos
Autores principales: Zaytseva, Anastasia, Tulintseva, Tatyana, Fomicheva, Yulya, Mikhailova, Valeria, Treshkur, Tatiana, Kostareva, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9044080/
https://www.ncbi.nlm.nih.gov/pubmed/35495129
http://dx.doi.org/10.3389/fgene.2022.718853

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9044080/
https://www.ncbi.nlm.nih.gov/pubmed/35495129
http://dx.doi.org/10.3389/fgene.2022.718853

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