Systematic Review of Clinical and Pathophysiological Features of Genetic Creutzfeldt–Jakob Disease Caused by a Val-to-Ile Mutation at Codon 180 in the Prion Protein Gene.

Autor: Matsubayashi, Taiki1 (AUTHOR), Sanjo, Nobuo1 (AUTHOR) n-sanjo.nuro@tmd.ac.jp
Zdroj: International Journal of Molecular Sciences. Dec2022, Vol. 23 Issue 23, p15172. 15p.
Databáze: Academic Search Ultimate
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