Dollfus,Hélène

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

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