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Article

Genetic bases and phenotypes of autosomal recessive Parkinson disease in a Turkish population.

European journal of neurology - 1 May 2012

Lohmann E, Dursun B, Lesage S, Hanagasi H A, Sevinc G, Honore A, Bilgic B, Gürvit H, Dogu O, Kaleagası H, Babacan G, Yazici J, Erginel-Unaltuna N, Brice A, Emre M

Abstract excerpt

BACKGROUND AND PURPOSE: To evaluate the phenotype and the frequencies of mutations in PRKN, DJ1 and PINK1 genes in patients with Parkinson disease (PD) in Turkey. METHODS: Eighty-six patients from 77 PD families participated in the study. Seventy-four families were originating from Turkey, two families from Greece and one family from Bulgaria. All patients underwent detailed neurological examination. PRKN, PINK1...

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Identifiers

PMID: 22233331
DOI: 10.1111/j.1468-1331.2011.03639.x

Genes

PRKN
PINK1

Variants

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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