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Article

A multidisciplinary study of patients with early-onset PD with and without parkin mutations.

Neurology - 13 Jan 2009

Lohmann E, Thobois S, Lesage S, Broussolle E, du Montcel S Tezenas, Ribeiro M-J, Remy P, Pelissolo A, Dubois B, Mallet L, Pollak P, Agid Y, Brice A

Abstract excerpt

OBJECTIVE: To establish phenotype-genotype correlations in early-onset Parkinson disease (EOPD), we performed neurologic, neuropsychological, and psychiatric evaluations in a series of patients with and without parkin mutations. BACKGROUND: Parkin (PARK2) gene mutations are the major cause of aut...

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Identifiers

PMID: 18987353
DOI: 10.1212/01.wnl.0000327098.86861.d4
PMCID: PMC2677494

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18987353-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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