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Unexpected phenotypic and molecular changes of combined glucocerebrosidase and acid sphingomyelinase deficiency. (2023)

First Author: Keatinge M

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/10.1242/dmm.049954

PubMed Identifier: 36951087

Publication URI: http://europepmc.org/abstract/MED/36951087

Type: Journal Article/Review

Volume: 16

Parent Publication: Disease models & mechanisms

Issue: 6

ISSN: 1754-8403