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Association of mutations in the glucocerebrosidase gene with Parkinson disease in a Korean population.

Neuroscience letters - 11 Apr 2012

Choi Jung Mi, Kim Won Chan, Lyoo Chul Hyoung, Kang Suk Yun, Lee Phil Hyu, Baik Jong Sam, Koh Seong-Beom, Ma Hyeo-Il, Sohn Young Ho, Lee Myung Sik, Kim Yun Joong

Abstract excerpt

Recent studies have shown an association between Parkinson disease (PD) and mutations in the gene encoding the lysosomal enzyme glucocerebrosidase (GBA), which is deficient in patients with Gaucher disease. In Asian populations, 2 mutational analysis studies have been performed in all exons of GBA; one study in a Japanese population showed the highest odds ratio among all ethnic groups, whereas the other study in...

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Identifiers

PMID: 22387070
DOI: 10.1016/j.neulet.2012.02.035

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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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