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Year | Number of Results |
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1994 | 1 |
2006 | 1 |
2008 | 1 |
2024 | 0 |
PubMed (cited) for id: 612422
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Cardiac troponin T mutation in familial cardiomyopathy with variable remodeling and restrictive physiology.
Clin Genet. 2008 Nov;74(5):445-54. doi: 10.1111/j.1399-0004.2008.01062.x. Epub 2008 Jul 21.
Clin Genet. 2008.
PMID: 18651846
Free PMC article.
Infantile restrictive cardiomyopathy resulting from a mutation in the cardiac troponin T gene.
Peddy SB, Vricella LA, Crosson JE, Oswald GL, Cohn RD, Cameron DE, Valle D, Loeys BL.
Peddy SB, et al.
Pediatrics. 2006 May;117(5):1830-3. doi: 10.1542/peds.2005-2301.
Pediatrics. 2006.
PMID: 16651346
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Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere.
Thierfelder L, Watkins H, MacRae C, Lamas R, McKenna W, Vosberg HP, Seidman JG, Seidman CE.
Thierfelder L, et al.
Cell. 1994 Jun 3;77(5):701-12. doi: 10.1016/0092-8674(94)90054-x.
Cell. 1994.
PMID: 8205619
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