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An integrated transcriptomics and proteomics analysis reveals functional endocytic dysregulation caused by mutations in LRRK2. (2019)

First Author: Connor-Robson N

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.nbd.2019.04.005

PubMed Identifier: 30954703

Publication URI: http://europepmc.org/abstract/MED/30954703

Type: Journal Article/Review

Volume: 127

Parent Publication: Neurobiology of disease

ISSN: 0969-9961