Case Report: Family Curse: An SCN5A Mutation, c.611C>A, p.A204E Associated With a Family History of Dilated Cardiomyopathy and Arrhythmia

OBJECTIVE: We report a 3-generation family with SCN5A c.611 C>A rare variant, whose clinical characteristics are dilated cardiomyopathy (DCM) combined with multifocal ectopic Purkinje-related premature contractions (MEPPC). We tried to explain why the same SCN5A variant carriers had different phe...

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Detalles Bibliográficos
Autores principales: Huang, Wen, Xu, Rui, Gao, Ning, Wu, Xia, Wen, Cong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Cardiovascular Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9120596/
https://www.ncbi.nlm.nih.gov/pubmed/35600473
http://dx.doi.org/10.3389/fcvm.2022.822150

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9120596/
https://www.ncbi.nlm.nih.gov/pubmed/35600473
http://dx.doi.org/10.3389/fcvm.2022.822150

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