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DYT1 mutation in a cohort of Taiwanese primary dystonias.

Parkinsonism & related disorders - 1 Jan 2006

Lin Yen-Wen, Chang Hsiu-Chen, Chou Yah-Huei Wu, Chen Rou-Shayn, Hsu Wen-Chi, Wu Wen-Shiang, Weng Yi-Hsin, Lu Chin-Song

Abstract excerpt

To investigate the DYT1 gene mutation in Chinese ethnic, we examined a series of 200 patients with primary dystonias (11 familial and 189 sporadic), 53 of their asymptomatic relatives, 97 patients with familial or early-onset parkinsonism, and 200 healthy subjects. The GAG deletion at codon 946 was only found in three sporadic dystonia patients and seven of their asymptomatic familial members. The frequency of...

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Identifiers

PMID: 16198613
DOI: 10.1016/j.parkreldis.2005.08.002

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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