A MYH7 variant in a five-generation-family with hypertrophic cardiomyopathy

A MYH7 variant in a five-generation-family with hypertrophic cardiomyopathy

Background: Hypertrophic cardiomyopathy (HCM) is a genetic condition with a prevalence of 1:500–1:3 000. Variants in genes encoding sarcomeric proteins are mainly responsible for the disease. MYH7 gene encoding a myosin heavy chain beta, together with MYPBC3 gene are the two most commonly affected g...

Full description

Bibliographic Details
Main Authors: Magda Franke, Tomasz Marcin Książczyk, Marta Dux, Przemysław Chmielewski, Grażyna Truszkowska, Dorota Czapczak, Radosław Pietrzak, Zofia Teresa Bilinska, Urszula Demkow, Bożena Werner
Format: Article
Language:English
Published: Frontiers Media S.A. 2024-02-01
Series:Frontiers in Genetics
Subjects:
hypertrophic cardiomyopathy
HCM
MYH7
variant
next-generation sequencing
Online Access:https://www.frontiersin.org/articles/10.3389/fgene.2024.1306333/full

Internet

https://www.frontiersin.org/articles/10.3389/fgene.2024.1306333/full

Similar Items