Abidi,Fatima E

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

Top Collaborators: 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, Raymond FL, Cox J

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