Hyderabad researchers have identified two rare MYH7 gene variants associated with hypertrophic cardiomyopathy in patients from Telangana. The findings, published in a leading cardiology journal, could support early diagnosis, precision medicine and family screening for inherited heart disease.
CCMB study finds “the genetic variants responsible for Covid-19 severity among Europeans may not play a role in Covid-19 susceptibility among South Asians”
