High prevalence of fulminant hepatic failure among patients with mutant alleles for truncation of ATP7B in Wilson's disease-Reference-Cited by-同舟云学术

High prevalence of fulminant hepatic failure among patients with mutant alleles for truncation of ATP7B in Wilson's disease

Published:2010-05-21 Issue:10 Volume:45 Page:1232-1237
ISSN:0036-5521
Container-title:Scandinavian Journal of Gastroenterology
language:en
Short-container-title:Scandinavian Journal of Gastroenterology

Author:

Okada Toshihide,Shiono Yuta,Kaneko Yoshibumi,Miwa Kazuhiro,Hasatani Kenkei,Hayashi Yoshiaki,Mibayashi Hiroshi,Aoyagi Hiroyuki,Tsuji Shigetsugu,Yoshimitsu Masashi,Hayashi Hisao,Yamagishi Masakazu

Publisher

Informa UK Limited

Subject

Gastroenterology

Link

http://www.tandfonline.com/doi/pdf/10.3109/00365521.2010.492527

Reference18 articles.

1. A genetical analysis of thirty families with Wilson's disease (hepatolenticular degeneration)

2. Scheinberg IH, Sternlieb I. Wilson's disease: major problems in internal medicine. In: Smith LH Jr, editor. Vol. XXII. Philadelphia: Saunders; 1984.

3. The Wilson disease gene is a putative copper transporting P–type ATPase similar to the Menkes gene

4. Presence of ATP-dependent copper transport in the hepatocyte canalicular membrane of the long-evans cinnamon rat, an animal model of wilson disease

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