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Results 1 - 10 of 116 for Hypertrophic cardiomyopathy 7
  1. ... Registry: Hypertrophic cardiomyopathy 4 Genetic Testing Registry: Hypertrophic cardiomyopathy 7 Familial hypertrophic cardiomyopathy National Organization for Rare Disorders ( ...
  2. ... PubMed Berko BA, Swift M. X-linked dilated cardiomyopathy. N Engl J Med. 1987 May 7;316(19):1186-91. doi: 10.1056/NEJM198705073161904. Citation on PubMed Cohen N, Muntoni F. Multiple pathogenetic mechanisms in X linked dilated cardiomyopathy. Heart. 2004 Aug;90(8):835-41. doi: ...
  3. ... sarcomere protein genes as a cause of dilated cardiomyopathy. N Engl J Med. 2000 Dec 7;343(23):1688-96. doi: 10.1056/NEJM200012073432304. ... heavy chain gene mutations in patients with hypertrophic cardiomyopathy. J Mol Med (Berl). 2005 ... Epub 2005 Apr 22. Citation on PubMed Rodriguez ...
  4. ... Morales A, Hershberger RE. Genetic evaluation of dilated cardiomyopathy. Curr Cardiol Rep. 2013 Jul;15(7):375. doi: 10.1007/s11886-013-0375-1. Citation on PubMed Posafalvi A, Herkert JC, Sinke RJ, van den Berg MP, ... gene card for: dilated cardiomyopathy (CMD). Eur J Hum Genet. 2013 Oct;21( ...
  5. ... VENTRICULAR NONCOMPACTION 10; LVNC10 CARDIOMYOPATHY, DILATED, 1R; CMD1R CARDIOMYOPATHY, DILATED, 1S; CMD1S LEFT VENTRICULAR NONCOMPACTION 7; LVNC7 PubMed Bennett CE, Freudenberger R. The Current ...
  6. ... role of mutations in the SCN5A gene in cardiomyopathies. Biochim Biophys Acta. 2016 Jul;1863(7 Pt B):1799-805. doi: 10.1016/j. ...
  7. ... and its deficiency causes centronuclear myopathy with dilated cardiomyopathy. Am J Hum Genet. 2014 Aug 7;95(2):218-26. doi: 10.1016/j. ...
  8. ... not a causative mutation in arrhythmogenic right ventricular cardiomyopathy. Eur J Hum Genet. 2010 Jul;18(7):776-82. doi: 10.1038/ejhg.2010.19. Epub 2010 Mar 3. Citation on PubMed or Free article on PubMed Central ... cardiomyopathy caused by desmocollin-2 mutations. Cardiovasc Res. 2011 ...
  9. ... JG, Seidman CE. Truncations of titin causing dilated cardiomyopathy. N Engl J Med. 2012 Feb 16;366(7):619-28. doi: 10.1056/NEJMoa1110186. Citation on ...
  10. ... 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. Epub 2012 ...
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