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Results 1 - 10 of 29 for Hypertrophic cardiomyopathy 12
  1. RAF1 gene 
    ... mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy. Nat Genet. 2007 Aug;39(8):1007-12. doi: 10.1038/ng2073. Epub 2007 Jul 1. ...
    https://medlineplus.gov/genetics/gene/raf1 - Genetics
  2. MYBPC3 gene 
    ... in the molecular genetics of left ventricular noncompaction cardiomyopathy. Clin Chim Acta. 2017 Feb;465:40-44. doi: 10.1016/j.cca.2016.12.013. Epub 2016 Dec 15. Citation on PubMed ...
    https://medlineplus.gov/genetics/gene/mybpc3 - Genetics
  3. MYH7 gene 
    ... in the molecular genetics of left ventricular noncompaction cardiomyopathy. Clin Chim Acta. 2017 Feb;465:40-44. doi: 10.1016/j.cca.2016.12.013. Epub 2016 Dec 15. Citation on PubMed ...
    https://medlineplus.gov/genetics/gene/myh7 - Genetics
  4. PKP2 gene 
    ... the molecular phenotype of two arrhythmogenic right ventricular cardiomyopathy (ARVC)-related plakophilin-2 (PKP2) mutations. Heart Rhythm. 2008 Dec;5(12):1715-23. doi: 10.1016/j.hrthm.2008. ...
    https://medlineplus.gov/genetics/gene/pkp2 - Genetics
  5. POMT1 gene 
    ... Bertini E, Angelini C, Tosatto SC, Pegoraro E. Cardiomyopathy in patients with POMT1-related congenital and limb-girdle muscular dystrophy. Eur J Hum Genet. 2012 Dec;20(12):1234-9. doi: 10.1038/ejhg.2012.71. ...
    https://medlineplus.gov/genetics/gene/pomt1 - Genetics
  6. PRKAG2 gene 
    ... A new mutation in PRKAG2 gene causing hypertrophic cardiomyopathy with conduction system disease and muscular glycogenosis. Neuromuscul Disord. 2006 Mar;16(3):178-82. doi: 10.1016/j.nmd.2005.12.004. Epub 2006 Feb 17. Citation on PubMed ...
    https://medlineplus.gov/genetics/gene/prkag2 - Genetics
  7. TNNI3 gene 
    ... j.yjmcc.2009.10.031. Epub 2009 Nov 12. Citation on PubMed Xu Q, Dewey S, Nguyen S, Gomes AV. Malignant and benign mutations in familial cardiomyopathies: insights into mutations linked to complex cardiovascular phenotypes. ...
    https://medlineplus.gov/genetics/gene/tnni3 - Genetics
  8. DMD gene 
    ... proteins, multiple phenotypes. Lancet Neurol. 2003 Dec;2(12):731-40. doi: 10.1016/s1474-4422(03)00585-4. Citation on PubMed Nakamura A. X-Linked Dilated Cardiomyopathy: A Cardiospecific Phenotype of Dystrophinopathy. Pharmaceuticals (Basel). 2015 ...
    https://medlineplus.gov/genetics/gene/dmd - Genetics
  9. FKTN gene 
    ... M, Nishino I. Fukutin gene mutations cause dilated cardiomyopathy with minimal muscle weakness. Ann ... Epub 2006 Feb 7. Citation on PubMed ...
    https://medlineplus.gov/genetics/gene/fktn - Genetics
  10. JUP gene 
    ... JUNCTION PLAKOGLOBIN; JUP ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 12; ARVD12 ... dominant mutation in plakoglobin causes arrhythmogenic right ventricular cardiomyopathy. Am J Hum Genet. 2007 Nov;81(5): ...
    https://medlineplus.gov/genetics/gene/jup - Genetics
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