Open AccessWhole‑exome sequencing reveals MYH7 p.R671C mutation in three different phenotypes of familial hypertrophic cardiomyopathy
Author(s) -
Wei Yu,
Mi-Mi Huang,
Guohong Zhang,
Wei Wang,
ChunJuan Chen,
Jidong Cheng
Publication year - 2021
Publication title -
experimental and therapeutic medicine
Language(s) - English
Resource type - Journals
eISSN - 1792-1015
pISSN - 1792-0981
DOI - 10.3892/etm.2021.10434
Subject(s) - myh7 , hypertrophic cardiomyopathy , proband , sanger sequencing , missense mutation , exome sequencing , genetics , medicine , sudden death , genetic counseling , exome , sudden cardiac death , genetic heterogeneity , cardiology , biology , mutation , phenotype , gene , gene isoform
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom