Abidi,Fatima E

Institution: Genetics of Learning Disability Service, Hunter Genetics, Waratah, New South Wales, Australia

Top Collaborators: Cox J, Stratton MR, Whibley A, Schwartz CE, Boyle J, Rogers C, Grigg J, Partington M, Stevenson RE, Tolmie J, Yates JR, Turner G, Wilson M, Futreal AP, Corbett M, Hackett A, Shaw M, Tarpey PS, Gecz J, Licata A

Research Interests: Calcium, Atrophy, Brainstem, Calmodulin, Congenital Nystagmus, Families, Gene, Kinase, Mental Retardation, Microcephaly, Missense Mutation, Missense Mutations, Mutation, Mutations, Optic Atrophy, Phenotype, Protein Kinase, Report, Serine, Syndrome