Novel <i>NKX2.5</i> variant associated with congenital heart disease and increased risk of malignant arrhythmia and sudden cardiac death.

Helm, Benjamin M; Baud, Rebecca; Shopp, Laura; Kean, Adam C; Ayers, Mark D

Novel NKX2.5 variant associated with congenital heart disease and increased risk of malignant arrhythmia and sudden cardiac death.

Helm, Benjamin M; Baud, Rebecca; Shopp, Laura; Kean, Adam C; Ayers, Mark D.

Afiliação

Helm BM; Department of Medical & Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN, USA.
Baud R; Department of Epidemiology, Indiana University Fairbanks School of Public Health, Indianapolis, IN, USA.
Shopp L; Department of Medical & Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN, USA.
Kean AC; Department Pediatrics, Division of Pediatric Cardiology, Indiana University School of Medicine, Indianapolis, IN, USA.
Ayers MD; Department Pediatrics, Division of Pediatric Cardiology, Indiana University School of Medicine, Indianapolis, IN, USA.

Cardiol Young ; 34(3): 654-658, 2024 Mar.

Article em En | MEDLINE | ID: mdl-37697673

Assuntos

Arritmias Cardíacas; Cardiopatias Congênitas; Humanos; Arritmias Cardíacas/genética; Morte Súbita Cardíaca/etiologia; Cardiopatias Congênitas/complicações; Cardiopatias Congênitas/genética; Coração; Doença do Sistema de Condução Cardíaco

Palavras-chave

CHD; NKX2.5; conduction disease; sudden cardiac death

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Arritmias Cardíacas / Cardiopatias Congênitas Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

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