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Heterozygous desmin gene (DES) mutation contributes to familial dilated cardiomyopathy

Familial dilated cardiomyopathy (FDCM) is characterized by high genetic heterogeneity and an increased risk of heart failure or sudden cardiac death in adults. We report the case of a 62-year-old man with a 2-month history of shortness of breath during activity, without paroxysmal nocturnal dyspnea....

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Detalles Bibliográficos
Autores principales:	Huang, Ying-shuo, Xing, Yun-li, Li, Hong-wei
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	SAGE Publications 2021
Materias:	Case Reports
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8033466/ https://www.ncbi.nlm.nih.gov/pubmed/33823640 http://dx.doi.org/10.1177/03000605211006598

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