Mutations in HTRA2 are not a common cause of familial classic ET.
作者信息
Hopfner Franziska, Müller Stefanie H, Lorenz Delia, Appenzeller Silke, Klebe Stephan, Deuschl Günther, Kuhlenbäumer Gregor
机构信息
Department of Neurology, University Hospital Schleswig Holstein, Kiel, Germany.
Core Unit Systems Medicine, University of Würzburg, Germany.
出版信息
Mov Disord. 2015 Jul;30(8):1149-50. doi: 10.1002/mds.26252. Epub 2015 May 13.
PMID:25970799
Abstract
摘要
Zotero 插件