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; 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;

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