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Mutations in the glucocerebrosidase gene and Parkinson disease: phenotype-genotype correlation.

Neurology - 8 Nov 2005

Aharon-Peretz Judith, Badarny Samih, Rosenbaum Hanna, Gershoni-Baruch Ruth

Abstract excerpt

Mutations in the glucocerebrosidase (GBA) gene have been recently identified as contributory to Parkinson disease (PD) in Ashkenazi Jews. In the present study, the clinical characteristics of Ashkenazi patients with PD with GBA mutations (n = 40) were compared to those of Ashkenazi patients with PD without any known GBA mutation (n = 108). The overall clinical manifestations and age at disease onset did not...

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Identifiers

PMID: 16148263
DOI: 10.1212/01.wnl.0000176987.47875.28

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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