Genotype-Phenotype Correlation in Hypertrophic Cardiomyopathy: New Variant p.Arg652Lys in MYH7
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DOI: 10.3390/genes13020320
Abstract: Hypertrophic cardiomyopathy (HCM) is a genetic disease characterised by increased left ventricle (LV) wall thickness caused by mutations in sarcomeric genes. Finding a causal mutation can help to better assess the proband’s risk, as it… read more here.
Keywords: hypertrophic cardiomyopathy; patients hcm; variant; arg652lys ... See more keywords