Double missense mutations in cardiac myosin‐binding protein C and myopalladin genes: A case report with diffuse coronary disease, complete atrioventricular block, and progression to dilated cardiomyopathy

Cardiomyopathies caused by double gene mutations are rare but conferred a remarkably increased risk of end‐stage progression, arrhythmias, and poor outcome. Compound genetic mutations leading to complex phenotype in the setting of cardiomyopathies represent an important challenge in clinical practic...

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Detalhes bibliográficos
Publicado no:Ann Noninvasive Electrocardiol
Main Authors: Mastroianno, Sandra, Palumbo, Pietro, Castellana, Stefano, Leone, Maria Pia, Massaro, Raimondo, Potenza, Domenico Rosario, Mazza, Tommaso, Russo, Aldo, Castori, Marco, Carella, Massimo, Di Stolfo, Giuseppe
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2019
Assuntos:
Case Reports
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7358828/
https://ncbi.nlm.nih.gov/pubmed/31524317
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/anec.12687
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