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Results 1 - 10 of 38 for Hypertrophic cardiomyopathy 4
  1. PKP2 gene 
    ... major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy. Circulation. 2006 Apr 4;113(13):1650-8. doi: 10.1161/CIRCULATIONAHA. ...
    https://medlineplus.gov/genetics/gene/pkp2 - Genetics
  2. MYH7 gene 
    ... mutations in contractile proteins cause the primary familial cardiomyopathies? J Cardiovasc Transl Res. 2011 Jun;4(3):245-55. doi: 10.1007/s12265-011- ...
    https://medlineplus.gov/genetics/gene/myh7 - Genetics
  3. TTN gene 
    ... cause a novel early-onset myopathy with fatal cardiomyopathy. Ann Neurol. 2007 Apr;61(4):340-51. doi: 10.1002/ana.21089. Erratum ... the giant muscle filament titin, cause familial dilated cardiomyopathy. Nat Genet. 2002 Feb;30(2):201-4. doi: 10.1038/ng815. Epub 2002 Jan 14. ...
    https://medlineplus.gov/genetics/gene/ttn - Genetics
  4. TNNT2 gene 
    ... of TNNT2 mutations identified in patients with dilated cardiomyopathy. Circ Cardiovasc Genet. 2009 Aug;2(4):306-13. doi: 10.1161/CIRCGENETICS.108.846733. ...
    https://medlineplus.gov/genetics/gene/tnnt2 - Genetics
  5. MYBPC3 gene 
    ... mutations in contractile proteins cause the primary familial cardiomyopathies? J Cardiovasc Transl Res. 2011 Jun;4(3):245-55. doi: 10.1007/s12265-011- ...
    https://medlineplus.gov/genetics/gene/mybpc3 - Genetics
  6. LAMP2 gene 
    ... Seidman JG. Glycogen storage diseases presenting as hypertrophic cardiomyopathy. N Engl J Med. 2005 Jan 27;352(4):362-72. doi: 10.1056/NEJMoa033349. Citation on ...
    https://medlineplus.gov/genetics/gene/lamp2 - Genetics
  7. TNNI3 gene 
    ... mutations in contractile proteins cause the primary familial cardiomyopathies? J Cardiovasc Transl Res. 2011 Jun;4(3):245-55. doi: 10.1007/s12265-011- ...
    https://medlineplus.gov/genetics/gene/tnni3 - Genetics
  8. GNPTAB gene 
    ... of mucolipidosis III associated with sensory neuropathy and cardiomyopathy. Am J Med Genet A. 2005 Feb 1;132A(4):369-75. doi: 10.1002/ajmg.a.30498. ...
    https://medlineplus.gov/genetics/gene/gnptab - Genetics
  9. ABCC9 gene 
    ... Terzic A. ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating. Nat Genet. 2004 Apr;36(4):382-7. doi: 10.1038/ng1329. Epub 2004 ...
    https://medlineplus.gov/genetics/gene/abcc9 - Genetics
  10. DNAJC19 gene 
    ... mutation of mitochondrial DNAJC19 causing dilated and noncompaction cardiomyopathy, anemia, ataxia, and male genital anomalies. Pediatr Res. 2012 Oct;72(4):432-7. doi: 10.1038/pr.2012.92. ...
    https://medlineplus.gov/genetics/gene/dnajc19 - Genetics
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