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Familial hypertrophic cardiomyopathy 8
- ... 6; CMH6 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 1; CMH1 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8; CMH8 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10; CMH10 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 25; ...
- ... HAIR AND KERATODERMA; DCWHK ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 8; ARVD8 EPIDERMOLYSIS BULLOSA, LETHAL ACANTHOLYTIC; EBLA CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS; ...
- ... Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy. Circulation. 2006 Apr 4;113(13):1650-8. doi: 10.1161/CIRCULATIONAHA.105.609719. Epub 2006 ...
- ... WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY; CPVT1 ... ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10; ARVD10 ...
- ... Jacobson Z, Young TL, Marshall JD, Kaplan P. Familial variable expression of dilated cardiomyopathy in Alstrom syndrome: a report of four sibs. Am J Med Genet A. 2005 May 15;135(1):96-8. doi: 10.1002/ajmg.a.30688. Citation on ...
- ... filaments. Science. 2012 Sep 7;337(6099):1215-8. doi: 10.1126/science.1223602. Epub 2012 Aug 23. Citation on PubMed or Free article on PubMed Central Rodriguez JE, McCudden CR, Willis MS. Familial hypertrophic cardiomyopathy: basic concepts and future molecular diagnostics. Clin Biochem. ...
- ... Novel mutations and genotype-phenotype relationships in 107 families with ... dilated cardiomyopathy with minimal muscle weakness. Ann Neurol. 2006 Nov; ...
- ... pointes. Circulation. 2002 Apr 23;105(16):1943-8. doi: 10.1161/01.cir.0000014448.19052.4c. ... Epub 2016 Feb 23. Citation on PubMed
- Familial dilated cardiomyopathy is a genetic form of heart disease. It occurs when heart (cardiac) muscle becomes thin and weakened in at least one chamber of ...
- ... Restrictive cardiomyopathies. Eur J Echocardiogr. 2009 Dec;10(8):iii23-33. doi: ... cardiomyopathies: insights into mutations linked to complex cardiovascular ...