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Article

Uncommon phenotype for a codon 178 mutation of the human PrP gene.

Annals of neurology - 1 Mar 1992

Laplanche J L, Chatelain J, Thomas S, Launay J M, Gaultier C, Derouesne C

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 1353344
DOI: 10.1002/ana.410310321

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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