Ventricular fibrillation in Graves disease reveals a rare SCN5A mutation with W1191X variant associated with Brugada syndrome

Detalles Bibliográficos
Autores principales: Stawiarski, Kristin, Clarke, John-Ross D., Pollack, Ari, Winslow, Robert, Majumdar, Sachin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7897746/
https://www.ncbi.nlm.nih.gov/pubmed/33665110
http://dx.doi.org/10.1016/j.hrcr.2020.11.010

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7897746/
https://www.ncbi.nlm.nih.gov/pubmed/33665110
http://dx.doi.org/10.1016/j.hrcr.2020.11.010

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