Genetically confirmed Wilson disease in a 9-month old boy with elevations of aminotransferases

Advanced Search

BPG is committed to discovery and dissemination of knowledge

Home / Archive / Volume 5, Issue 3

This Article

Citation of this article

Corresponding Author of This Article

Article-Type of This Article

Open-Access Policy of This Article

Times Cited Counts in Google of This Article

Number of Hits and Downloads for This Article

All Articles published online

Item

Count

PDF

416

HTML

3093

Figures (1-4)

191

Tables (1-1)

171

Sum=3871

Mar 27, 2013 (publication date) through Aug 31, 2024

Times Cited of This Article

Journal Information of This Article

Publication Name

World Journal of Hepatology

ISSN

1948-5182

Publisher of This Article

Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

Case Report

World J Hepatol. Mar 27, 2013; 5(3): 156-159
Published online Mar 27, 2013. doi: 10.4254/wjh.v5.i3.156

Full Size Figure Download Figure

Figure 4 Pedigree. The patient has a compound heterozygote of p.G1186S and c.4006delA.

Citation: Kim JW, Kim JH, Seo JK, Ko JS, Chang JY, Yang HR, Kang KH. Genetically confirmed Wilson disease in a 9-month old boy with elevations of aminotransferases. World J Hepatol 2013; 5(3): 156-159
URL: https://www.wjgnet.com/1948-5182/full/v5/i3/156.htm
DOI: https://dx.doi.org/10.4254/wjh.v5.i3.156