緩徐な臨床経過後に急速進行性認知機能障害を呈し E200K 変異にコドン 219Lys 多型を伴った遺伝性 Creutzfeldt-Jakob disease の 1 例

Translated title of the contribution: Genetic Creutzfeldt-Jakob disease with a glutamate-to-lysine substitution at codon 219 (E219K) in the presence of the E200K mutation presenting with rapid progressive dementia following slowly progressive clinical course

Mika Takayanagi, Keisuke Suzuki, Toshiki Nakamura, Koichi Hirata, Katsuya Satoh, Tetsuyuki Kitamoto

Research output: Contribution to journalArticlepeer-review

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Medicine & Life Sciences