Variation p.R1045H in MYH7 correlated with hypertrophic cardiomyopathy in a Chinese pedigree

• Auteurs principaux: Yan Zhang (Auteur), Yiyi Shang (Auteur), Luo Liu (Auteur), Xiaoxue Ding (Auteur), Haiyan Wu (Auteur), Lijiang Li (Auteur), Mingjie Pang (Auteur)
• Format: Livre
• Publié: BMC, 2021-07-01T00:00:00Z.
• Sujets: article
• Accès en ligne: Connect to this object online.

Abstract Background Inherited hypertrophic cardiomyopathy (HCM) is a common heart muscle disease that damages heart function and may cause the heart to suddenly stop beating. Genetic factors play an important role in HCM. Pedigree analysis is a good way to identify the genetic defects that cause dis...