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11. Co-existence of frataxin and cardiac troponin T gene mutations in a child with Friedreich Ataxia and familial hypertrophic cardiomyopathy. Cuda G; Mussari A; Concolino D; Costanzo FS; Strisciuglio P Hum Mutat; 2002 Mar; 19(3):309-10. PubMed ID: 11857753 [TBL] [Abstract][Full Text] [Related]
12. Clinical features of hypertrophic cardiomyopathy caused by an Arg278Cys missense mutation in the cardiac troponin T gene. Theopistou A; Anastasakis A; Miliou A; Rigopoulos A; Toutouzas P; Stefanadis C Am J Cardiol; 2004 Jul; 94(2):246-9. PubMed ID: 15246915 [TBL] [Abstract][Full Text] [Related]
14. Recent advances in the molecular genetics of hypertrophic cardiomyopathy. Marian AJ; Roberts R Circulation; 1995 Sep; 92(5):1336-47. PubMed ID: 7648684 [No Abstract] [Full Text] [Related]
15. Diagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in Danish hypertrophic cardiomyopathy patients and relatives. Andersen PS; Havndrup O; Hougs L; Sørensen KM; Jensen M; Larsen LA; Hedley P; Thomsen AR; Moolman-Smook J; Christiansen M; Bundgaard H Hum Mutat; 2009 Mar; 30(3):363-70. PubMed ID: 19035361 [TBL] [Abstract][Full Text] [Related]
16. How should hypertrophic cardiomyopathy be classified?: Molecular diagnosis for hypertrophic cardiomyopathy: Not ready for prime time. Elliott P; McKenna WJ Circ Cardiovasc Genet; 2009 Feb; 2(1):87-9; discussion 89. PubMed ID: 20031570 [No Abstract] [Full Text] [Related]
17. [Clinical and molecular genetics of hypertrophic cardiomyopathy]. Sepp R; Csanády M Orv Hetil; 1998 Aug; 139(33):1965-71. PubMed ID: 9734214 [TBL] [Abstract][Full Text] [Related]
18. Cardiomyopathy: molecular and immunological aspects (review). Takeda N Int J Mol Med; 2003 Jan; 11(1):13-6. PubMed ID: 12469210 [TBL] [Abstract][Full Text] [Related]
19. Symposium on gene abnormalities in medical diseases. 3. Molecular genetics of hypertrophic cardiomyopathy in Japan. Kimura A Intern Med; 1997 Feb; 36(2):152-4. PubMed ID: 9099608 [No Abstract] [Full Text] [Related]
20. Cardiac troponin T mutations in Chinese patients with hypertrophic cardiomyopathy. Wu HF; Yang D; Wan WH; Bian ZP; Xu JD; Ma WZ; Zhang JN Chin Med J (Engl); 2004 Jun; 117(6):944-6. PubMed ID: 15198905 [No Abstract] [Full Text] [Related] [Next] [New Search]