Variant Gerstmann-Sträussler syndrome with the P105L prion gene mutation: an unusual case with nigral degeneration and widespread neurofibrillary tangles
M. Yamazaki, Kiyomitsu Oyanagi, Osamu Mori, Shin Kitamura, Masashi Ohyama, Akiro Terashi, Tetsuyuki Kitamoto, Yasuo KatayamaVolume:
98
Language:
english
Pages:
6
DOI:
10.1007/s004010051116
Date:
September, 1999
File:
PDF, 581 KB
english, 1999