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Mitochondrial dysfunction associated with glucocerebrosidase deficiency. (2016)

First Author: Gegg ME

Attributed to: Glucocerebrosidase mutations in Parkinson disease:molecular pathogenesis,and the basis for personalised therapy with small molecule chaperones funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.nbd.2015.09.006

PubMed Identifier: 26388395

Publication URI: http://europepmc.org/abstract/MED/26388395

Type: Journal Article/Review

Volume: 90

Parent Publication: Neurobiology of disease

ISSN: 0969-9961