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Biegstraaten M., van Schaik I.N., Aerts J.M., Hollak C.E. Non-neuronopathic Gaucher disease reconsidered. Prevalence of neuronological manifestations in a Ducth cohort of type 1 Gaucher disease patients and a systematic review of the literature. J. Inher. Metab. Dis. 2008, 31:337-349.
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Schulte, C.48
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The association between mutations in the lysosomal protein glucocerebrosidase and Parkinsonism
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Neuropathology provides clues to the pathophysiology of Gaucher disease
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Wong K., Sidransky E., Vernia A., Mixon T., Sandberg G.D., Wakefield L.K., Morrison A., Lwin A., Colegial C., Allman J.M., Schiffmann R. Neuropathology provides clues to the pathophysiology of Gaucher disease. Molec. Genet. Metab. 2004, 82:192-207.
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Glucocerebrosidase is present in a-synuclein inclusions in Lewy body disorders
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Goker-Alpan O., Stubblefield B.K., Giasson B.I., Sidransky E. Glucocerebrosidase is present in a-synuclein inclusions in Lewy body disorders. Acta Neuropathol. 2010, 120:641-649.
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Glucocerebrosidase gene mutations and Parkinson disease in the Norwegian population
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Genotype phenotype correlations between GBA mutations and Parkinson disease risk and onset
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Haplotype analysis suggests a single Balkan origin for the Gaucher disease [D409H:H255Q] double mutant allele
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Homozygosity for the double D409H:H255Q allele in type II Gaucher disease
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Glucocerebrosidase mutation T369M appears to be another polymorphism
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