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Article

A comprehensive analysis of deletions, multiplications, and copy number variations in PARK2.

Neurology - 28 Sept 2010

Kay D M, Stevens C F, Hamza T H, Montimurro J S, Zabetian C P, Factor S A, Samii A, Griffith A, Roberts J W, Molho E S, Higgins D S, Gancher S, Moses L, Zareparsi S, Poorkaj P, Bird T, Nutt J, Schellenberg G D, Payami H

Abstract excerpt

OBJECTIVES: To perform a comprehensive population genetic study of PARK2. PARK2 mutations are associated with juvenile parkinsonism, Alzheimer disease, cancer, leprosy, and diabetes mellitus, yet ironically, there has been no comprehensive study of PARK2 in control subjects; and to resolve contro...

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Source

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Identifiers

PMID: 20876472
DOI: 10.1212/WNL.0b013e3181f4d832
PMCID: PMC3013490

Genes

APOE
MAPT
SNCA

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-20876472-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

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

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