Mohammed Bennaceur

<i>KVLQT1</i> C-Terminal Missense Mutation Causes a Forme Fruste Long-QT Syndrome

Claire Donger, Isabelle Denjoy, Myriam Berthet et al. · Circulation · 1997 · 347 citations

Medicine, Cardiology, Genetics +16

Clinical Features and Prognostic Implications of Familial Hypertrophic Cardiomyopathy Related to the Cardiac Myosin-Binding Protein C Gene

Philippe Charron, Olivier Dubourg, Michel Desnos et al. · Circulation · 1998 · 282 citations · Full text

Life Sciences, Cardiology, Genetics +14

Genotype-phenotype analysis in four families with mutations in β-myosin heavy chain gene responsible for familial hypertrophic cardiomyopathy

Frédérique Tesson, Pascale Richard, Philippe Charron et al. · Human Mutation · 1998 · 46 citations

Life Sciences, Cardiology, Genetics +13

Exclusion of KCNE1 (IsK) as a Candidate Gene for Jervell and Lange-Nielsen Syndrome

Frédérique Tesson, Claire Donger, Isabelle Denjoy et al. · Journal of Molecular and Cellular Cardiology · 1996 · 44 citations

Life Sciences, Genetics, Molecular Genetics +10