Variable clinical manifestation of a novel missense mutation in the alpha-tropomyosin (TPM1) gene in familial hypertrophic cardiomyopathy

Autor: Jongbloed, Roselie J.1,2 roselie.jongbloed@gen.unimaas.nl, Marcelis, Carlo L.3, Doevendans, Pieter A.3,4, Schmeitz-Mulkens, Judith M.3, Van Dockum, Willem G.4,5, Geraedts, Joep P.1,3, Smeets, Hubert J.1
Zdroj: Journal of the American College of Cardiology (JACC). Mar2003 Supplement, Vol. 41, p981. 6p.
Databáze: Academic Search Ultimate