Copper toxicosis gene MURR1 is not changed in Wilson disease patients with normal blood ceruloplasmin levels

Advanced Search

BPG is committed to discovery and dissemination of knowledge

Home / Archive / Volume 12, Issue 14

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

228

HTML

1986

Figures (1-2)

134

Tables (1-1)

119

Sum=2467

Apr 14, 2006 (publication date) through Apr 24, 2024

Times Cited of This Article

Journal Information of This Article

Publication Name

World Journal of Gastroenterology

ISSN

1007-9327

Publisher of This Article

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

Rapid Communication

World J Gastroenterol. Apr 14, 2006; 12(14): 2239-2242
Published online Apr 14, 2006. doi: 10.3748/wjg.v12.i14.2239

Figure 1 Mean ceruloplasmin blood levels in patients with two or less identified mutated alleles of ATP7B.

Figure 2 Map of the human MURR1 gene. Localization of the reported polymorphism (492 T > C) in exon 3 is marked.

Citation: Weiss KH, Merle U, Schaefer M, Ferenci P, Fullekrug J, Stremmel W. Copper toxicosis gene MURR1 is not changed in Wilson disease patients with normal blood ceruloplasmin levels. World J Gastroenterol 2006; 12(14): 2239-2242
URL: https://www.wjgnet.com/1007-9327/full/v12/i14/2239.htm
DOI: https://dx.doi.org/10.3748/wjg.v12.i14.2239