- Haplotype analysis and possible founder effect at the R778L mutation of the ATP7B gene in Korean patients with Wilson's disease
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Bae SH, Kim JW, Seo JK
- KMID: 1374959
- Korean J Hepatol.
- 2009 Sep;15(3):309-319.
- doi: 10.3350/kjhep.2009.15.3.309
BACKGROUND/AIMS: Wilson's disease (WD) is an inherited disorder of copper metabolism caused by alteration of the P-type adenosine triphosphatase (ATP) 7B gene. In this study, we analyzed the frequency of... -
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