Rare genetic E196A mutation in a patient with Creutzfeldt-Jakob disease: a case report and literature

Wu, XP; Cui, Z; Xie, GM; Wang, HF; Zhang, XL; Li, ZG; Sun, Q; Qi, FT

Wu, XP; Xie, GM (corresponding author), Li Huili Hosp, Ningbo Med Ctr, Dept Neurol, 1111 Jiangnan Rd, Ningbo, Peoples R China.

PRION, 2020; 14 (1): 143

Abstract

Genetic Creutzfeldt-Jakob disease (gCJD) is characterized by mutations in the PRNP gene and represents approximately 10-15% of the human prion disease......

Full Text Link


Links

期刊讨论 | 中国SCI论文 | 期刊主页 | 投稿经验 | 杂志官网 | 投稿链接 | 作者需知 | PMC链接 | Pubmed全文检索