A Family with Myh7 Mutation and Different Forms of Cardiomyopathies.

Bianca Iulia CatrinaFlorina BatarGeorgiana BaltatCornel Ioan BiteaAndreea PuiaOana StoiaSorin-Radu Fleacă Minodora Teodoru

Published in: Biomedicines (2023)

Our results reveal three variants in phenotypes of cardiomyopathies in a family with MYH7 mutation associated with high SCD risk and ICD needed for primary and secondary prevention.

Keyphrases

hypertrophic cardiomyopathy
copy number
genome wide
single cell
left ventricular
heart failure
gene expression