Variant Gerstmann-Sträussler syndrome with the P105L prion gene mutation: an unusual case with nigral degeneration and widespread neurofibrillary tangles

✍ Scribed by M. Yamazaki; Kiyomitsu Oyanagi; Osamu Mori; Shin Kitamura; Masashi Ohyama; Akiro Terashi; Tetsuyuki Kitamoto; Yasuo Katayama

• Book ID: 106075771
• Publisher: Springer-Verlag
• Year: 1999
• Tongue: English
• Weight: 581 KB
• Volume: 98
• Category: Article
• ISSN: 0001-6322
• DOI: 10.1007/s004010051116