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Article

Abnormal visual gain control in a Parkinson's disease model.

Human molecular genetics - 1 Sept 2014

Afsari Farinaz, Christensen Kenneth V, Smith Garrick Paul, Hentzer Morten, Nippe Olivia M, Elliott Christopher J H, Wade Alex R

Abstract excerpt

Our understanding of Parkinson's disease (PD) has been revolutionized by the discovery of disease-causing genetic mutations. The most common of these is the G2019S mutation in the LRRK2 kinase gene, which leads to increased kinase activity. However, the link between increased kinase activity and...

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Identifiers

PMID: 24718285
DOI: 10.1093/hmg/ddu159
PMCID: PMC4119403

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24718285-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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