Genotype-Phenotype Relations for Isolated Dystonia Genes: MDSGene Systematic Review.

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第一作者： Lara M,Lange

第一单位： Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.

作者： Lara M,Lange ^[1] ; Johanna,Junker ^[2] ; Sebastian,Loens ^[2] ; Hauke,Baumann ^[1] ; Luisa,Olschewski ^[1] ; Susen,Schaake ^[1] ; Harutyun,Madoev ^[1] ; Sonja,Petkovic ^[1] ; Neele,Kuhnke ^[1] ; Meike,Kasten ^[3] ; Ana,Westenberger ^[1] ; Aloysius,Domingo ^[4] ; Connie,Marras ^[5] ; Inke R,König ^[6] ; Sarah,Camargos ^[7] ; Laurie J,Ozelius ^[8] ; Christine,Klein ^[2] ; Katja,Lohmann ^[1]

作者单位： Institute of Neurogenetics, University of Lübeck, Lübeck, Germany. ^[1] Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.;Department of Neurology, University of Lübeck, Lübeck, Germany. ^[2] Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.;Department of Psychiatry and Psychotherapy, University of Lübeck, Lübeck, Germany. ^[3] Center for Genomic Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA. ^[4] The Morton and Gloria Shulman Movement Disorders Centre and the Edmond J Safra Program in Parkinson's Disease, Toronto Western Hospital, University of Toronto, Toronto, Ontario, Canada. ^[5] Institute of Medical Biometry and Statistics, University of Lübeck, Lübeck, Germany. ^[6] Movement Disorders Unit, Neurology Service, Internal Medicine Department, Hospital das Clínicas, The Federal University of Minas Gerais, Belo Horizonte, Brazil. ^[7] Department of Neurology, Harvard Medical School and Massachusetts General Hospital, Charlestown, Massachusetts, USA. ^[8]

关键词 ANO3 GNAL HPCA KMT2B PRKRA THAP1 TOR1A dystonia movement disorder