Genetic Study of Hypertrophic Cardiomyopathy in Iranian children: The Role of a De novo Variant

Background and Objectives: Hypertrophic cardiomyopathy is a common cardiac disease diagnosed in young adults and rarely detectable in childhood. Hypertrophic cardiomyopathy exhibits considerable diversity in its clinical and genetic characteristics. To date, mutations in multiple genes associated wi...

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Autores principales:	Arastoo Kaki, Mohammad Dalili, Nejat Mahdieh, Mehrdad Noruzinia
Formato:	Artigo
Lenguaje:	Persa
Publicado:	Hamadan University of Medical Sciences 2023-09-01
Colección:	پژوهان
Materias:	hypertrophic cardiomyopathy children whole exome sequencing myh7 mybpc3
Acceso en línea:	http://psj.umsha.ac.ir/article-1-1025-en.pdf
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