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: Ross, S. B., Bagnall, R. D., Ingles, J., Van Tintelen, J. P., Semsarian, C. Tags: Genetics, Cardiomyopathy, Hypertrophy Original Articles Source Type: research
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