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Article

PINK1 mutation in Taiwanese early-onset parkinsonism : clinical, genetic, and dopamine transporter studies.

Journal of neurology - 1 Oct 2007

Weng Yi-Hsin, Chou Yah-Huei Wu, Wu Wen-Shiang, Lin Kun-Ju, Chang Hsiu-Chen, Yen Tzu-Chen, Chen Rou-Shayn, Wey Shiaw-Pyng, Lu Chin-Song

Abstract excerpt

The PINK1 gene mutation is probably the second most common genetic cause of early-onset Parkinson's disease (EOPD). The frequency and the characteristics of the PINK1 mutation in the Taiwanese population are unknown. This study was designed to investigate the genotype, phenotype and dopaminergic function of PINK1 in a cohort of EOPD patients. The genetic settings were to detect the PINK1 gene mutations in 138...

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Source

Identifiers

PMID: 17960343
DOI: 10.1007/s00415-007-0534-7

Genes

PINK1

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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