Ventricular fibrillation in Graves disease reveals a rare <i>SCN5A</i> mutation with W1191X variant associated with Brugada syndrome.

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.

Stawiarski, Kristin; Clarke, John-Ross D; Pollack, Ari; Winslow, Robert; Majumdar, Sachin.

Afiliación

Stawiarski K; Yale New Haven Health Heart and Vascular Center, Bridgeport Hospital, Bridgeport, Connecticut.
Clarke JD; Yale New Haven Health Heart and Vascular Center, Bridgeport Hospital, Bridgeport, Connecticut.
Pollack A; Yale New Haven Health Heart and Vascular Center, Bridgeport Hospital, Bridgeport, Connecticut.
Winslow R; Yale New Haven Health Heart and Vascular Center, Bridgeport Hospital, Bridgeport, Connecticut.
Majumdar S; Yale New Haven Health Heart and Vascular Center, Bridgeport Hospital, Bridgeport, Connecticut.

HeartRhythm Case Rep ; 7(2): 95-99, 2021 Feb.

Article en En | MEDLINE | ID: mdl-33665110

Palabras clave

Arrhythmias; Brugada syndrome; Genetic mutation; Hyperthyroidism; Implantable cardioverter-defibrillator; Ventricular fibrillation

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: HeartRhythm Case Rep Año: 2021 Tipo del documento: Article

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google