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

Publication URI: http://dx.doi.org/10.1002/mds.29385

Type: Journal Article/Review

Parent Publication: Movement Disorders

Issue: 6