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A Swedish family with de novo α-synuclein A53T mutation: Evidence for early cortical dysfunction

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第一作者： Puschmann,A.

作者： Puschmann,A. ^[1] ; Ross,O.A. ^[2] ; Vilari?o-Güell,C. ^[3] ; Lincoln,S.J. ^[4] ; Kachergus,J.M. ^[5] ; Cobb,S.A. ^[6] ; Lindquist,S.G. ^[7] ; Nielsen,J.E. ^[8] ; Wszolek,Z.K. ^[9] ; Farrer,M. ^[10] ; Widner,H. ^[11] ; vanWesten,D. ; H?gerstr?m,D. ; Markopoulou,K. ; Chase,B.A. ; Nilsson,K. ; Reimer,J. ; Nilsson,C.

作者单位： Institute of Cellular and Molecular Medicine, Section of Neurogenetics, University of Copenhagen ^[1] Department of Clinical Neurophysiology, Lund University Hospital, Sweden ^[2] Department of Neuroscience, Mayo Clinic, Jacksonville, FL, United States ^[3] Department of Radiology, Lund University Hospital, Sweden ^[4] Department of Clinical Science, Section of Geriatric Psychiatry, Lund University, Sweden ^[5] Department of Neurology, Lund University Hospital, Sweden, Department of Clinical Science, Section ^[6] University of Thessaly, Medical School, Larissa, Greece ^[7] Department of Biology, University of Nebraska at Omaha, Omaha, NE, United States ^[8] Department of Neurology, Lund University Hospital, Sweden ^[9] Department of Neurology, Mayo Clinic, Jacksonville, FL, United States ^[10] Division of Neurogenetics, Rigshospitalet Copenhagen University Hospital, Denmark ^[11]