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The New p.F1700L LRRK2 Variant Causes Parkinson's Disease by Extensively Increasing Kinase Activity. (2023)

First Author: Borsche M

Attributed to: Understanding Signalling Pathways Mutated in Inherited Disorders funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1002/mds.29385

PubMed Identifier: 36971062

Publication URI: http://europepmc.org/abstract/MED/36971062

Type: Journal Article/Review

Volume: 38

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

Issue: 6

ISSN: 0885-3185