Creutzfeldt–Jakob disease with homozygous M232R mutation: A case report

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Bibliographic Details
Published in:Journal of the neurological sciences 2015-05, Vol.352 (1), p.108-109
Main Authors: Kon, Tomoya, Miki, Yasuo, Arai, Akira, Funamizu, Yukihisa, Ueno, Tatsuya, Haga, Rie, Nishijima, Haruo, Suzuki, Chieko, Nunomura, Jin-ichi, Baba, Masayuki, Oyama, Yoshinobu, Shiga, Yusei, Kitamoto, Tetsuyuki, Tomiyama, Masahiko
Format: Article
Language:English
Subjects:
Brain - pathology
Creutzfeldt-Jakob Syndrome - diagnosis
Creutzfeldt-Jakob Syndrome - genetics
Creutzfeldt-Jakob Syndrome - pathology
Creutzfeldt–Jakob disease
Homozygote
Homozygous mutation
Humans
M232R
Male
Middle Aged
Mutation
Neurology
Polymorphism
Prion protein gene
Prions - genetics
Substitution
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ISSN:0022-510X
1878-5883
DOI:10.1016/j.jns.2015.03.017