Bondurand,Nadège

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

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

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