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
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author Stawiarski, Kristin
Clarke, John-Ross D.
Pollack, Ari
Winslow, Robert
Majumdar, Sachin
author_facet Stawiarski, Kristin
Clarke, John-Ross D.
Pollack, Ari
Winslow, Robert
Majumdar, Sachin
author_sort Stawiarski, Kristin
collection PubMed
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spelling pubmed-78977462021-03-03 Ventricular fibrillation in Graves disease reveals a rare SCN5A mutation with W1191X variant associated with Brugada syndrome Stawiarski, Kristin Clarke, John-Ross D. Pollack, Ari Winslow, Robert Majumdar, Sachin HeartRhythm Case Rep Case Report Elsevier 2020-11-20 /pmc/articles/PMC7897746/ /pubmed/33665110 http://dx.doi.org/10.1016/j.hrcr.2020.11.010 Text en © 2020 Heart Rhythm Society. Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Stawiarski, Kristin
Clarke, John-Ross D.
Pollack, Ari
Winslow, Robert
Majumdar, Sachin
Ventricular fibrillation in Graves disease reveals a rare SCN5A mutation with W1191X variant associated with Brugada syndrome
title Ventricular fibrillation in Graves disease reveals a rare SCN5A mutation with W1191X variant associated with Brugada syndrome
title_full Ventricular fibrillation in Graves disease reveals a rare SCN5A mutation with W1191X variant associated with Brugada syndrome
title_fullStr Ventricular fibrillation in Graves disease reveals a rare SCN5A mutation with W1191X variant associated with Brugada syndrome
title_full_unstemmed Ventricular fibrillation in Graves disease reveals a rare SCN5A mutation with W1191X variant associated with Brugada syndrome
title_short Ventricular fibrillation in Graves disease reveals a rare SCN5A mutation with W1191X variant associated with Brugada syndrome
title_sort ventricular fibrillation in graves disease reveals a rare scn5a mutation with w1191x variant associated with brugada syndrome
topic Case Report
url 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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AT majumdarsachin ventricularfibrillationingravesdiseaserevealsararescn5amutationwithw1191xvariantassociatedwithbrugadasyndrome

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