Burden of Recurrent and Ancestral Mutations in Families With Hypertrophic Cardiomyopathy [Original Articles]

Conclusions— The majority of families with a causal variant identified have a nonunique variant. Discovery of the genetic origins of human disease forms a fundamental basis for improved understanding of disease pathogenesis and phenotype development.
Source: Circulation: Cardiovascular Genetics - Category: Cardiology Authors: Tags: Genetics, Cardiomyopathy, Hypertrophy Original Articles Source Type: research