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Benign hereditary chorea related to NKX2.1: expansion of the genotypic and phenotypic spectrum
Authors:Kathryn J Peall  Daniel Lumsden  Rachel Kneen  Rajesh Madhu  Deirdre Peake  Frances Gibbon  Hilary Lewis  Tammy Hedderly  Esther Meyer  Stephanie A Robb  Bryan Lynch  Mary D King  Jean‐Pierre Lin  Huw R Morris  Heinz Jungbluth  Manju A Kurian
Affiliation:1. MRC Centre for Neuropsychiatric Genetics and Genomics, Institute of Psychological Medicine & Clinical Neurosciences, Cardiff University, , Cardiff, UK;2. Department of Paediatric Neurology, Evelina Children's Hospital, St Thomas' Hospital, , London, UK;3. Roald Dahl EEG Department, Alder Hey Children's Hospital, , Liverpool, UK;4. Royal Belfast Hospital for Sick Children, , Belfast, UK;5. Department of Paediatric Neurology, University Hospital of Wales, , Cardiff, UK;6. Department of Paediatrics, Royal Gwent Hospital, , Newport, UK;7. ICH‐Neurosciences Unit, University College London, , London, UK;8. Dubowitz Neuromuscular Centre, Great Ormond Street Hospital, , London, UK;9. Paediatric Neurology, Children's University Hospital, , Dublin, Ireland
Abstract:
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