Bondurand,Nadege

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

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