The Association between E326K of GBA and the Risk of Parkinson’s Disease

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A molecular analysis of theGBAgene in Caucasian South Africans with Parkinson's disease

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Strong association between glucocerebrosidase mutations and Parkinson's disease in Sweden

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Mutations in glucocerebrosidase are a major genetic risk factor for Parkinson’s disease and increase susceptibility to dementia in a Flanders-Belgian cohort

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GBA Variants Influence Motor and Non-Motor Features of Parkinson’s Disease

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Association ofGBAMutations and the E326K Polymorphism With Motor and Cognitive Progression in Parkinson Disease

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Mutations in the glucocerebrosidase gene are common in patients with Parkinson's disease from Eastern Canada

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Parkinson's disease

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Effect ofGBAMutations on Phenotype of Parkinson’s Disease: A Study on Chinese Population and aMeta-Analysis

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Mutations in the glucocerebrosidase gene are responsible for Chinese patients with Parkinson’s disease

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Clinicogenetic study of GBA mutations in patients with familial Parkinson's disease

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The glucocerobrosidase E326K variant predisposes to Parkinson's disease, but does not cause Gaucher's disease

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The enigma of the E326K mutation in acid β-glucocerebrosidase

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Mutations in the glucocerebrosidase gene confer a risk for Parkinson disease in North Africa

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Critical evaluation of the Newcastle-Ottawa scale for the assessment of the quality of nonrandomized studies in meta-analyses

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Mutations for Gaucher Disease Confer High Susceptibility to Parkinson Disease

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Complete screening for glucocerebrosidase mutations in Parkinson disease patients from Greece

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Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease

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Gaucher disease: mutation and polymorphism spectrum in the glucocerebrosidase gene (GBA)

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Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onset

(2008) W. C. Nichols et al.   NEUROLOGY

Complete screening for glucocerebrosidase mutations in Parkinson disease patients from Portugal

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Association between Parkinson's disease and glucocerebrosidase mutations in Brazil

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