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Glucocerebrosidase and Parkinson disease: Recent advances

Mutations of the glucocerebrosidase (GBA) gene are the most important risk factor yet discovered for Parkinson disease (PD). Homozygous GBA mutations result in Gaucher disease (GD), a lysosomal storage disorder. Heterozygous mutations have not until recently been thought to be associated with any pa...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Mol Cell Neurosci
Prif Awdur: Schapira, A.H.V.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2015
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC4471139/
https://ncbi.nlm.nih.gov/pubmed/25802027
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mcn.2015.03.013
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