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Article

Rare E196K mutation in the PRNP gene of a patient exhibiting behavioral abnormalities.

Clinical neurology and neurosurgery - 1 Apr 2010

Béjot Yannick, Osseby Guy-Victor, Caillier Marie, Moreau Thibault, Laplanche Jean-Louis, Giroud Maurice

Abstract excerpt

Genetic transmissible spongiform encephalopathies (TSEs) account for approximately 10-15% of overall human prion diseases worldwide, but genotype-phenotype correlations remain incomplete. Here we report the case of an 80-year-old man who developed rapidly progressive behavioral abnormalities and...

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Source

Identifiers

PMID: 20005032
DOI: 10.1016/j.clineuro.2009.11.002

Genes

PRNP

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20005032-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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