Reply: PRKAR1B mutations are a rare cause of FUS negative neuronal intermediate filament inclusion disease

• 期刊名称Brain
• 作者Wong, Tsz Hang; Verkerk, Annemieke J. M. H.; Rozemuller, Annemieke J.; Willemsen, Rob; Neumann, Manuela; Bonifati, Vincenzo; van Swieten, John
• 卷第138卷
• 期第6期
• 印刷ISSN0006-8950
• 电子ISSN1460-2156
• 文件大小131.53KB
• 发表时间2015-06
• DOI10.1093/brain/awu333