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Periventricular heterotopia in 6q terminal deletion syndrome: Role of the C6orf70 gene

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第一作者: Conti,V.
作者单位: NIHR Biomedical Research Centre, Wellcome Trust Centre for Human Genetics, Oxford, OX3 7BN, United [1] Department of Paediatrics and Child Health, Dunedin School of Medicine, University of Otago [2] Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Parkville, VIC 3052 [3] Department of Neurology, Royal Children's Hospital, Parkville, VIC 3052, Australia, Murdoch [4] INSERM, INMED UMR901, Parc Scientifique de Luminy, BP 13, 13273 Marseille, France, UniversitéAix [5] Plateforme postgenomique INMED-INSERM, Parc Scientifique de Luminy, BP 13, 13273, Marseille, France [6] Epilepsy Research Centre, Department of Medicine, University of Melbourne, VIC 3010, Australia [7] Genetic Medicine, St Mary's Hospital, University of Manchester, Manchester M13 9WL, United Kingdom [8] Centre for Integrative Brain Research, Seattle Children's Research Institute, Seattle WA 98101 [9] Department of Clinical Genetics, Oxford Radcliffe NHS Trust, Oxford OX3 9DU, United Kingdom [10] Department Molecular Medicine, University of Pavia, 27100, Pavia, Italy [11] Paediatric Neurology and Muscular Diseases Unit, Department of Neurosciences, Rehabilitation [12] Department Molecular Medicine, University of Pavia, 27100, Pavia, Italy, IRCCS Casimiro Mondino [13] Research Institute of Molecular Pathology, 1030, Vienna, Austria [14] Paediatric Neurology and Neurogenetics Unit and Laboratories, A. Meyer Children's Hospital [15]
发布时间 2014-02-27
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Brain: A journal of neurology

Brain

2013年136卷11期

3378-3394页

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