A case of hemochromatosis due to heterozygous mutations in <i>TfR2</i>-Reference-Cited by-同舟云学术

A case of hemochromatosis due to heterozygous mutations in <i>TfR2</i>

Published:2022-03-01 Issue:3 Volume:63 Page:151-157
ISSN:0451-4203
Container-title:Kanzo
language:en
Short-container-title:Acta hepatologica Japonica

Author:

Nishio Hitoshi¹,Honma Yuichi¹,Kumamoto Keiichiro¹,Toki Yasumichi²,Morino Kahori¹,Oe Shinji¹,Miyagawa Koichiro¹,Shibata Michihiko¹,Abe Shintaro¹,Tatsumi Yasuaki³,Ikuta Katsuya²,Hayashi Hisao³,Harada Masaru¹

Affiliation:

1. Third Department of Internal Medicine, School of Medicine, University of Occupational and Environmental Health

2. Division of Gastroenterology and Hematology/Oncology, Department of Medicine, Asahikawa Medical University

3. Laboratory of Medicine, Aichi-Gakuin University, School of Pharmacy

Publisher

Japan Society of Hepatology

Subject

Hepatology

Link

https://www.jstage.jst.go.jp/article/kanzo/63/3/63_151/_pdf

Reference21 articles.

1. 1) Powell LW, Seckington RC, Deugnier Y. Haemochromatosis. Lancet 2016; 388: 706-716

2. 2) Ikuta K, Hatayama M, Addo L, et al. Iron overload patients with unknown etiology from national survey in Japan. Int J Hematol 2017; 105: 353-360

3. 3) Pietrangelo A. Hereditary hemochromatosis: pathogenesis, diagnosis, and treatment. Gastroenterology 2010; 139: 393-408

4. 4) Bomford A. Genetics of haemochromatosis. Lancet 2002; 360: 1673-1681

5. 5) Hayashi H, Wakusawa S, Motonishi S, et al. Genetic background of primary iron overload syndromes in Japan. Intern Med 2006; 45: 1107-1111

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