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Article

Lack of association between PRNP M129V polymorphism and multiple sclerosis, mild cognitive impairment, alcoholism and schizophrenia in a Korean population.

Disease markers - 1 Jan 2010

Choi Ihn-Geun, Woo Sung-Il, Kim Ho Jin, Kim Dai-Jin, Park Byung Lae, Cheong Hyun Sub, Pasaje Charisse Flerida A, Park Tae Joon, Bae Joon Seol, Chai Young Gyu, Shin Hyoung Doo

Abstract excerpt

The genetic variant at codon 129 (M129V) of the prion protein gene (PRNP) is considered to be a major genetic risk factor for prion diseases. In this study, we examined the possible genetic association of PRNP*129Val with multiple sclerosis (MS, n=681), mild cognitive impairment (MCI, n=801), alcoholism (n=761) and schizophrenia (n=715) in a Korean population, and compared the data with previous genetic...

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Source

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Identifiers

PMID: 20592456
DOI: 10.3233/DMA-2010-0711
PMCID: PMC3833710

Genes

PRNP
MAF

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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