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Article

Mutation analysis of Taiwanese Wilson disease patients.

Biochemical and biophysical research communications - 30 Jun 2006

Wan Lei, Tsai Chang-Hai, Tsai Yuhsin, Hsu Chin-Moo, Lee Cheng-Chun, Tsai Fuu-Jen

Abstract excerpt

Wilson disease (WD) is an autosomal recessive disorder of copper metabolism, which is caused by mutation in copper-transporting ATPase (ATP7B). In the present study, we report a molecular diagnosis method to screen the WD chromosome in patients or in heterozygotic carriers in Taiwan. Exons 8, 11,...

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Identifiers

PMID: 16696937
DOI: 10.1016/j.bbrc.2006.04.136

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-16696937-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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