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The influence of the angiotensin I converting enzyme genotype in familial hypertrophic cardiomyopathy varies with the disease gene mutation

Tesson F.; Dufour C.; Moolman J.C.; Carrier L.; Al-Mahdawi S.; Chojnowska L.; Dubourg O.; Soubrier F.; Brink P.; Komajda M.; Guicheney P.; Schwartz K.; Feingold J. (1997)

Familial hypertrophic cardiomyopathy is an autosomal dominant genetically heterogeneous disease characterized by a partial penetrance and variable expressivity. Previous studies showed that the extent of hypertrophy is ...