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

• Principais autores: Yan Zhang (Autor), Yiyi Shang (Autor), Luo Liu (Autor), Xiaoxue Ding (Autor), Haiyan Wu (Autor), Lijiang Li (Autor), Mingjie Pang (Autor)
• Formato: Livro
• Publicado em: BMC, 2021-07-01T00:00:00Z.
• Assuntos: article
• Acesso em linha: 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...