Clinical features of genetic Creutzfeldt-Jakob disease with V180I mutation in the prion protein gene-Reference-Cited by-同舟云学术

Clinical features of genetic Creutzfeldt-Jakob disease with V180I mutation in the prion protein gene

Published:2014-05 Issue:5 Volume:4 Page:e004968
ISSN:2044-6055
Container-title:BMJ Open
language:en
Short-container-title:BMJ Open

Author:

Qina Temu,Sanjo Nobuo,Hizume Masaki,Higuma Maya,Tomita Makoto,Atarashi Ryuichiro,Satoh Katsuya,Nozaki Ichiro,Hamaguchi Tsuyoshi,Nakamura Yosikazu,Kobayashi Atsushi,Kitamoto Tetsuyuki,Murayama Shigeo,Murai Hiroyuki,Yamada Masahito,Mizusawa Hidehiro

Publisher

BMJ

Subject

General Medicine

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4. Prospective 10-year surveillance of human prion diseases in Japan;Nozaki;Brain,2010

5. Relationships between clinicopathological features and cerebrospinal fluid biomarkers in Japanese patients with genetic prion diseases;Higuma;PLoS ONE,2013

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