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Article

Identification and characterization of a novel endogenous murine parkin mutation.

Journal of neurochemistry - 1 Apr 2010

Ramsey Chenere P, Giasson Benoit I

Abstract excerpt

Various mutations in the PARK2 gene which encodes the protein, parkin, are causal of a disease entity-termed autosomal recessive juvenile parkinsonism. Parkin can function as an E3 ubiquitin-protein ligase, mediating the ubiquitination of specific targeted proteins and resulting in proteasomal de...

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Identifiers

PMID: 20089136
DOI: 10.1111/j.1471-4159.2010.06605.x
PMCID: PMC2908247

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20089136-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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