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  1. Oct 2023
  2. pubmed.ncbi.nlm.nih.gov pubmed.ncbi.nlm.nih.gov
    Genetic analysis of monoallelic double MYH7 mutations responsible for familial hypertrophic cardiomyopathy
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    1. luisaferero 22 Oct 2023
      MYH7-V934A, MYH7-E1387K and MYH7-M877I were identified as novel MYH7 mutations causing HCM.

      Novel mutations related to Hypertrophic cardiomyopathy using exome-sequencing technology and verified by Sanger

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    pubmed.ncbi.nlm.nih.gov/31638223/