Novel trans-2,3-enoyl-CoA reductase-like variant associated with catecholaminergic polymorphic ventricular tachycardia type 3.

Charafeddine, Fatme; Assaf, Nada; Ismail, Ali; Bulbul, Ziad

Charafeddine, Fatme; Assaf, Nada; Ismail, Ali; Bulbul, Ziad.

Afiliación

Charafeddine F; Department of Pediatrics and Adolescent Medicine, American University of Beirut Medical Center, Beirut, Lebanon.
Assaf N; Department of Pathology and Lab Medicine, American University of Beirut Medical Center, Beirut, Lebanon.
Ismail A; Department of Pediatrics and Adolescent Medicine, American University of Beirut Medical Center, Beirut, Lebanon.
Bulbul Z; Department of Pediatrics and Adolescent Medicine, American University of Beirut Medical Center, Beirut, Lebanon.

HeartRhythm Case Rep ; 9(3): 171-177, 2023 Mar.

Article en En | MEDLINE | ID: mdl-36970382

Palabras clave

CPVT; Inherited channelopathy; Long QT syndrome; Sudden cardiac death; TECRL

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: HeartRhythm Case Rep Año: 2023 Tipo del documento: Article País de afiliación: Líbano Pais de publicación: Estados Unidos

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