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RT @JesicaMRamirez: Next paper present a family broad clinical spectrum of HCM with MYH7 mutation. @FrontGenetics https://t.co/SgNbRGuMS9
RT @JesicaMRamirez: Next paper present a family broad clinical spectrum of HCM with MYH7 mutation. @FrontGenetics https://t.co/SgNbRGuMS9
Next paper present a family broad clinical spectrum of HCM with MYH7 mutation. @FrontGenetics https://t.co/SgNbRGuMS9
New Research: 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… https://t.co