Advances in GBA-associated Parkinson's disease – Pathology, presentation and therapies

GBA mutations are to date the most common genetic risk factor for Parkinson's disease. The GBA gene encodes the lysomal hydrolase glucocerebrosidase. Whilst bi-allelic GBA mutations cause Gaucher disease, both mono- and bi-allelic mutations confer risk for Parkinson's disease. Clinically,...

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Bibliographic Details
Published in:Neurochemistry international, Vol. 93 (2016), p. 6-25
Main Author: Barkhuizen, Melinda
Other Involved Persons: Anderson, David G. ; Grobler, Anne F.
Format: electronic Article
Language:English
ISSN:1872-9754
Physical Description:Online-Ressource
DOI:10.1016/j.neuint.2015.12.004
Other Editions:Show all 2 Editions
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