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Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere.
Cell. 1994 Jun 3;77(5):701-12. doi: 10.1016/0092-8674(94)90054-x.
Cell. 1994.
PMID: 8205619
Cardiac troponin T mutation in familial cardiomyopathy with variable remodeling and restrictive physiology.
Menon SC, Michels VV, Pellikka PA, Ballew JD, Karst ML, Herron KJ, Nelson SM, Rodeheffer RJ, Olson TM.
Menon SC, et al.
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.
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