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Genetic analysis of monoallelic double MYH7 mutations responsible for familial hypertrophic cardiomyopathy

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1. keahnacastillo 05 Feb 2026
  
  in Public
  
  The variants confirmed in this family were MYH7-A934V and MYH7-E1387K (Fig. 3A).
  
  Variants that cause HCM.
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pmc.ncbi.nlm.nih.gov/articles/PMC6854592/