A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia

作者:Galimberti D; Villa C; Ghezzi L; Pietroboni A; Fenoglio C; Cortini F; Serpente M; Cantoni C; Ridolfi E; Marcone A; Benussi L; Ghidoni R; Jacini F; Arighi A; Fumagalli G; Mandelli A; Binetti G; Cappa S; Bresolin N; Scarpini E
来源:21st Meeting of the European-Neurological-Society, 2011-05-28 to 2011-05-31.
  • 出版日期2011-5