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Whole-Exome Sequencing Reveals Mutational Signature of Hypertrophic Cardiomyopathy

BACKGROUND: Hypertrophic cardiomyopathy (HCM) is an extremely insidious and lethal disease caused by genetic variation. It has been studied for nearly 70 years since its discovery, but its cause of the disease remains a mystery. This study is aimed to explore the genetic pathogenesis of HCM in order...

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Detalles Bibliográficos
Autores principales:	Wang, Xi-Qin, Yuan, Fang, Yu, Bao-Rui
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Dove 2023
Materias:	Original Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10577257/ https://www.ncbi.nlm.nih.gov/pubmed/37850193 http://dx.doi.org/10.2147/IJGM.S422598

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