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
ISSN: 08853185
Editorial
WILEY, 111 RIVER ST, HOBOKEN 07030-5774, NJ, Estados Unidos America
Tipo de documento: Article
Volumen: 31 Número: 7
Páginas: 1033-1040
WOS Id: 000379942900019
ID de PubMed: 27061943
imagen Open Access

MÉTRICAS