Rare MYH7 Gene Variants Linked to Heart Disease
Our Science Reporter Hyderabad: Scientists from Hyderabad have identified two novel and rare genetic variants in the MYH7 gene associated with hypertrophic cardiomyopathy (HCM), an inherited heart condition that causes abnormal thickening of the heart muscle and can potentially lead to heart failure and sudden cardiac death. The discovery could strengthen efforts towards early diagnosis,…
