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Variable clinical manifestation of a novel missense mutation in the alpha-tropomyosin (TPM1) gene in familial hypertrophic cardiomyopathy.
J Am Coll Cardiol. 2003 Mar 19;41(6):981-6. doi: 10.1016/s0735-1097(02)03005-x.
J Am Coll Cardiol. 2003.
PMID: 12651045
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