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Glucocerebrosidase mutations and synucleinopathies: Toward a model of precision medicine. (2019)

First Author: Blandini F

Attributed to: JPND GBA1 mutations in Parkinson disease: clinical and biochemical prodrome, risk profile and pathogenetic modelling for therapeutic intervention. funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1002/mds.27583

PubMed Identifier: 30589955

Publication URI: http://europepmc.org/abstract/MED/30589955

Type: Journal Article/Review

Volume: 34

Parent Publication: Movement disorders : official journal of the Movement Disorder Society

Issue: 1

ISSN: 0885-3185