Hereditary hemochromatosis caused by a C282Y/H63D mutation in the HFE gene: A case report-Reference-Cited by-同舟云学术

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Hereditary hemochromatosis caused by a C282Y/H63D mutation in the HFE gene: A case report

Published:2024-04 Issue:7 Volume:10 Page:e28046
ISSN:2405-8440
Container-title:Heliyon
language:en
Short-container-title:Heliyon

Author:

Li Dongdong,Li Jinfeng,Zhang Hongkun,Zhu Qiuyu,Wang Teng,Zhao Wen,Zhao Shousong,Li Wei^ORCID

Publisher

Elsevier BV

Reference34 articles.

1. The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22;Camaschella;Nat. Genet.,2000

2. Expression of hepcidin is down-regulated in TfR2 mutant mice manifesting a phenotype of hereditary hemochromatosis;Kawabata;Blood,2005

3. The molecular genetics of haemochromatosis;Le Gac;European journal of human genetics,2005

4. Hereditary hemochromatosis: pathogenesis, diagnosis, and treatment;Pietrangelo;Gastroenterology,2010

5. A novel mammalian iron-regulated protein involved in intracellular iron metabolism;Abboud;J. Biol. Chem.,2000

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Genetic Correlation of HBB, HFE and HAMP Genes to Endocrinal Complications in Egyptian Beta Thalassemia Major Patients;Biochemical Genetics;2024-07-02

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