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Journal of Medical Genetics|August 16, 2003
Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutationsP Sébillon, C Bouchier, L D Bidot, et al.
British Journal of Sports Medicine|October 26, 2012
Significance of deep T-wave inversions in asymptomatic athletes with normal cardiovascular examinations: practical solutions for managing the diagnostic conundrumM G Wilson, S Sharma, F Carré, et al.
Circulation|June 19, 1998
Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to the cardiac myosin-binding protein C geneP Charron, O Dubourg, M Desnos, et al.
Human Mutation|November 26, 1998
Genotype-phenotype analysis in four families with mutations in beta-myosin heavy chain gene responsible for familial hypertrophic cardiomyopathyF Tesson, P Richard, P Charron, et al.
European Journal of Medical Genetics|July 3, 2019
Secondary findings from next generation sequencing: Psychological and ethical issues. Family and patient perspectivesF Houdayer, O Putois, M L Babonneau, et al.
European Heart Journal|October 26, 1999
Identification of a genetic risk factor for idiopathic dilated cardiomyopathy. Involvement of a polymorphism in the endothelin receptor type A gene. CARDIGENE groupP Charron, F Tesson, O Poirier, et al.
Revue Neurologique|April 20, 2024
Transthyretin amyloid polyneuropathy in France: A cross-sectional study with 413 patients and real-world tafamidis meglumine use (2009-2019)D Adams, P Cintas, G Solé, et al.
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