Genetic Evaluation Of Cardiomyopathies In Qatar Identifies Novel Sarcomere Gene Variants And Founder Arabic Mutations For The Disease

Mohammed Alhashemi, Kholoud Al Shafai,Chidambaram Manickam,Rania Musa,Najeeb Syed, Senthli Selvaraj,Fazulur Vempalli,Magdi Yacoub,Xavier Estivill

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY（2020）

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摘要

Hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM) are life threatening diseases described by abnormal structure and function of the heart muscle in the absence of any secondary causes. Various genetic mutations were found to cause to HCM and DCM, mostly following autosomal dominant

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novel sarcomere genetic variants,cardiomyopathies,qatar,mutations

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