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ArticleNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2026

E200K genetic Creutzfeldt-Jakob disease with codon 129 MV heterozygosity presenting with a V2-like phenotype: a case report.

Rui Sun et al.PubMed ↗Publisher ↗

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Full record →Abstract, authors, funding and every citing paper · PMID 42503537