Results 1 -
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145
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Hypertrophic cardiomyopathy 6
- ... HYPERTROPHIC, 3; CMH3 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4; CMH4 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6; CMH6 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 1; CMH1 CARDIOMYOPATHY, FAMILIAL ...
- ... alpha myosin, heavy polypeptide 6, cardiac muscle, alpha (cardiomyopathy, hypertrophic 1) myosin-6 SSS3 Tests of MYH6 PubMed MYOSIN, HEAVY CHAIN 6, CARDIAC MUSCLE, ALPHA; MYH6 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 14; CMH14 CARDIOMYOPATHY, DILATED, 1EE; CMD1EE ...
- ... mutations lead to the features of familial hypertrophic cardiomyopathy. More About This Health Condition At least six mutations in the MYH7 gene have been found ...
- Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) (American Academy of Family Physicians)Cardiomyopathy/Specifics ... Cardiomyopathy ... Arrhythmia/Specifics ... Arrhythmia ... Congenital Heart Defects/Specifics ... Congenital Heart Defects ... American Academy of Family ...
- ... S, Syrris P, McKenna WJ. Genetics of restrictive cardiomyopathy. Heart Fail Clin. 2010 Apr;6(2):179-86. doi: 10.1016/j.hfc.2009.11.005. Citation on PubMed Xu Q, Dewey S, Nguyen S, Gomes AV. ... insights into mutations linked to complex cardiovascular phenotypes. ...
- ... mutations in desmoplakin causes arrhythmogenic right ventricular dysplasia/cardiomyopathy. Circ Res. 2006 Sep 15;99(6):646-55. doi: 10.1161/01.RES.0000241482. ...
- ... complex contribution of TTN truncating variants to dilated cardiomyopathy. Circ Cardiovasc Genet. 2013 Apr;6(2):144-53. doi: 10.1161/CIRCGENETICS.111. ...
- ... S, Syrris P, McKenna WJ. Genetics of restrictive cardiomyopathy. Heart Fail Clin. 2010 Apr;6(2):179-86. doi: 10.1016/j.hfc. ...
- ... T, Zareba W. Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the task force criteria. Circulation. 2010 Apr 6;121(13):1533-41. doi: 10.1161/CIRCULATIONAHA. ...
- ... B. Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathy. Am J Hum Genet. 2006 Dec;79(6):1081-8. doi: 10.1086/509044. Epub 2006 ...