Abidi,Fatima E

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

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

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