Dollfus,Hélène

Institution: Laboratoire de Génétique Médicale, INSERM U1112, Fédération de Médecine Translationnelle de Strasbourg (FMTS), Université de Strasbourg, Strasbourg, France

Top Collaborators: Marion V, Stoetzel C, Danse JM, Verloes A, Schaefer E, Durand M, Hellé S, Mandel JL, Sigaudy S, Claussmann A, Flori E, Bonneau D, Pelletier V, Bitoun P, Goldenberg A, Muller J, Vincent MC, Mockel A, Messaddeq N, De Melo C

Research Interests: Syndrome, Bardet-biedl Syndrome, Obesity, Patients, Gene, Retinitis, Retinitis Pigmentosa, Cilia, Polydactyly, Proteins, Mutations, Report, Genes, Kidney, Cilium, Disease, Mutation, Association, Diseases, Adipogenesis