- Analysis of 12 Chinese Patients with Proline-to-Leucine Mutation at Codon 102-Associated Gerstmann-Sträussler-Scheinker Disease
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Wang J, Xiao K, Zhou W, Shi Q, Dong XP
- KMID: 2467732
- J Clin Neurol.
- 2019 Apr;15(2):184-190.
- doi: 10.3988/jcn.2019.15.2.184
BACKGROUND AND PURPOSE: Gerstmann-Sträussler-Scheinker disease (GSS) with a proline-to-leucine mutation at codon 102 (P102L) in the PRNP gene is the most frequently reported GSS subtype worldwide. This study aimed to... -
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