Hereditary hemochromatosis in a male patient with TFR2 (1861_1872del12) gene mutation: the second biopsy 19 years after diagnosis-Reference-Cited by-同舟云学术

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Hereditary hemochromatosis in a male patient with TFR2 (1861_1872del12) gene mutation: the second biopsy 19 years after diagnosis

Published:2011 Issue:11 Volume:52 Page:745-752
ISSN:0451-4203
Container-title:Kanzo
language:ja
Short-container-title:Kanzo

Author:

Kawanaka Miwa,Nakamura Jun,Oka Yoshihito,Kimura Tomonari,Goto Daisuke,Yamato Ryumei,Nishino Ken,Suehiro Mitsuhiko,Kawamoto Hirofumi,Yamada Gotaro,Hattori Ai,Hayashi Hisao

Publisher

Japan Society of Hepatology

Subject

Hepatology

Link

http://www.jstage.jst.go.jp/article/kanzo/52/11/52_11_745/_pdf

Reference17 articles.

1. A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis

2. Understanding iron homeostasis through genetic analysis of hemochromatosis and related disorders

3. Hereditary Hemochromatosis — A New Look at an Old Disease

4. AVAQ 594-597 deletion of the TfR2 gene in a Japanese family with hemochromatosis

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