Rare genetic Creutzfeldt-Jakob disease with E196A mutation: a case report

Dai, YY; Lang, Y; Ding, MX; Zhang, BZ; Han, XO; Duan, GY; Cui, L

Cui, L (reprint author), Jilin Univ, Hosp 1, Dept Neurol, Neurosci Ctr, Xinmin St 71, Changchun 130021, Jilin, Peoples R China.

PRION, 2019; 13 (1): 132

Abstract

Genetic Creutzfeldt-Jakob disease (gCJD) accounts for approximately 10-15% of human prion diseases. It is an autosomal dominant disease caused by miss......

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