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Identification of a genetic risk factor for idiopathic dilated cardiomyopathy. Involvement of a polymorphism in the endothelin receptor type A gene. CARDIGENE group.
Charron P, Tesson F, Poirier O, Nicaud V, Peuchmaurd M, Tiret L, Cambien F, Amouyel P, Dubourg O, Bouhour J, Millaire A, Juilliere Y, Bareiss P, André-Fouët X, Pouillart F, Arveiler D, Ferrières J, Dorent R, Roizès G, Schwartz K, Desnos M, Komajda M. Charron P, et al. Eur Heart J. 1999 Nov;20(21):1587-91. doi: 10.1053/euhj.1999.1696. Eur Heart J. 1999. PMID: 10529327
Organization and sequence of human cardiac myosin binding protein C gene (MYBPC3) and identification of mutations predicted to produce truncated proteins in familial hypertrophic cardiomyopathy.
Carrier L, Bonne G, Bährend E, Yu B, Richard P, Niel F, Hainque B, Cruaud C, Gary F, Labeit S, Bouhour JB, Dubourg O, Desnos M, Hagège AA, Trent RJ, Komajda M, Fiszman M, Schwartz K. Carrier L, et al. Among authors: bouhour jb. Circ Res. 1997 Mar;80(3):427-34. Circ Res. 1997. PMID: 9048664
Penetrance of familial hypertrophic cardiomyopathy.
Charron P, Carrier L, Dubourg O, Tesson F, Desnos M, Richard P, Bonne G, Guicheney P, Hainque B, Bouhour JB, Mallet A, Feingold J, Schwartz K, Komajda M. Charron P, et al. Among authors: bouhour jb. Genet Couns. 1997;8(2):107-14. Genet Couns. 1997. PMID: 9219008
139 results