Glucocerebrosidase and its relevance to Parkinson disease
Abstract
Mutations in GBA1, the gene encoding the lysosomal enzyme glucocerebrosidase, are among the most common known genetic risk factors for the development of Parkinson disease and related synucleinopathies. A great deal is known about GBA1, as mutations in GBA1 are causal for the rare autosomal storage disorder Gaucher disease. Over the past decades, significant progress has been made in understanding the genetics and cell biology of...
Paper Details
Title
Glucocerebrosidase and its relevance to Parkinson disease
Published Date
Aug 29, 2019
Journal
Volume
14
Issue
1
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