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A pathogenic variant in RAB32 causes autosomal dominant Parkinson's disease and activates LRRK2 kinase. (2024)

First Author: Gustavsson EK

Attributed to: Defining and diagnosing neurodegenerative Movement Disorders through integrated analysis of Genetics And neuroPathology (MD-GAP) funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1101/2024.01.17.24300927

PubMed Identifier: 38293014

Publication URI: http://europepmc.org/abstract/MED/38293014

Type: Journal Article/Review

Parent Publication: medRxiv : the preprint server for health sciences