Phenotypic insights into ADCY5-associated disease
Por:
Chang FC, Westenberger A, Dale RC, Smith M, Pall HS, Pérez-Dueñas B, Grattan-Smith P, Ouvrier RA, Mahant N, Hanna BC, Hunter M, Lawson JA, Max C, Sachdev R, Meyer E, Crimmins D, Pryor D, Morris JG, Münchau A, Grozeva D, Carss KJ, Raymond L, Kurian MA, Klein C and Fung VS
Publicada:
1 jul 2016
Ahead of Print:
8 abr 2016
Resumen:
Filiaciones:
Chang FC:
Movement Disorders Unit, Department of Neurology, Westmead Hospital, Sydney, Australia
Westenberger A:
Institute of Neurogenetics, University of Lübeck, Lübeck, Germany
Dale RC:
TY Nelson Department of Neurology and Neurosurgery, Children's Hospital at Westmead, Westmead, Australia
University of Sydney, Sydney, Australia
Smith M:
Department of Neurology, Birmingham Children's Hospital, Birmingham, United Kingdom
Pall HS:
College of Medical and Dental Studies, University of Birmingham, Birmingham, United Kingdom
Pérez-Dueñas B:
Molecular Neurosciences, Developmental Neurosciences Program, Institute of Child Health, University College London, London, United Kingdom
Department of Child Neurology, Sant Joan de Déu Hospital, University of Barcelona, Spain
Grattan-Smith P:
TY Nelson Department of Neurology and Neurosurgery, Children's Hospital at Westmead, Westmead, Australia
Ouvrier RA:
TY Nelson Department of Neurology and Neurosurgery, Children's Hospital at Westmead, Westmead, Australia
Mahant N:
Sydney Medical School, University of Sydney, Australia
Hanna BC:
Hunter Genetics, John Hunter Hospital, Newcastle, Australia
Hunter M:
Hunter Genetics, John Hunter Hospital, Newcastle, Australia
Genetics of Learning Disability Service, Newcastle, Australia
Lawson JA:
Sydney Children's Hospitals Network, Randwick, Australia
Max C:
Institute of Neurogenetics, University of Lübeck, Lübeck, Germany
Sachdev R:
Department of Medical Genetics, Sydney Children's Hospital, Randwick, Australia
Meyer E:
Molecular Neurosciences, Developmental Neurosciences Program, Institute of Child Health, University College London, London, United Kingdom
Crimmins D:
Neurology Department, Gosford Hospital, Gosford, Australia
Pryor D:
Neurology Department, St George Hospital, Kogarah, Australia
Morris JG:
Movement Disorders Unit, Department of Neurology, Westmead Hospital, Sydney, Australia
Münchau A:
Institute of Neurogenetics, University of Lübeck, Lübeck, Germany
Grozeva D:
Department of Medical Genetics, Cambridge Institute for Medical Research, University of Cambridge, Cambridge, United Kingdom
Carss KJ:
Department of Haematology, University of Cambridge, NHS Blood and Transplant Center, Cambridge, United Kingdom
Wellcome Trust Sanger Institute, Hinxton, Cambridge, United Kingdom
Raymond L:
Department of Medical Genetics, Cambridge Institute for Medical Research, University of Cambridge, Cambridge, United Kingdom
Kurian MA:
Molecular Neurosciences, Developmental Neurosciences Program, Institute of Child Health, University College London, London, United Kingdom
Klein C:
Institute of Neurogenetics, University of Lübeck, Lübeck, Germany
Fung VS:
Movement Disorders Unit, Department of Neurology, Westmead Hospital, Sydney, Australia
Sydney Medical School, University of Sydney, Australia
Open Access
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