Bondurand,Nadege

Institution: INSERM, U955, Equipe11, Créteil, France; Université Paris Est, Faculté de Médecine, Créteil, France

Top Collaborators: Goossens M, Pingault V, Chaoui A, Watanabe Y, Baral V, Marlin S, Vérier-mine O, Ente D, Francannet C, Dastot-le Moal F, Dupin-deguine D, Archambeaud F, Kurtz FJ, Stanchina L, Young J, Van De Putte T, Bertherat J, Huylebroeck D, Hardelin JP, Dodé C

Research Interests: Syndrome, Disease, Genes, Hirschsprung Disease, Pigmentation, Waardenburg Syndrome, Mutations, Association, Deafness, Mutation, Patients, Hearing, Hearing Loss, Sensorineural Hearing Loss, Transcription Factor, Nervous System, Phenotype, Transcription Factors, Patient, Point Mutations