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Results 1 - 5 of 5 for Primary familial hypertrophic cardiomyopathy
  1. TNNT2 gene 
    ... How do mutations in contractile proteins cause the primary familial cardiomyopathies? J Cardiovasc Transl Res. 2011 Jun;4(3): ...
    https://medlineplus.gov/genetics/gene/tnnt2 - Genetics
  2. TNNI3 gene 
    ... How do mutations in contractile proteins cause the primary familial cardiomyopathies? J Cardiovasc Transl Res. 2011 Jun;4(3): ...
    https://medlineplus.gov/genetics/gene/tnni3 - Genetics
  3. MYH7 gene 
    ... How do mutations in contractile proteins cause the primary familial cardiomyopathies? J Cardiovasc Transl Res. 2011 Jun;4(3): ...
    https://medlineplus.gov/genetics/gene/myh7 - Genetics
  4. MYBPC3 gene 
    ... How do mutations in contractile proteins cause the primary familial cardiomyopathies? J Cardiovasc Transl Res. 2011 Jun;4(3): ...
    https://medlineplus.gov/genetics/gene/mybpc3 - Genetics
  5. LAMP2 gene 
    ... Bonilla E, Nonaka I, DiMauro S, Hirano M. Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease). Nature. 2000 Aug 24; ...
    https://medlineplus.gov/genetics/gene/lamp2 - Genetics