Ferroportin Disease Caused by a Heterozygous Variant p.Cys326Phe in the SLC40A1 Gene and the Efficacy of Therapeutic Phlebotomy in Children-Reference-Cited by-同舟云学术

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Ferroportin Disease Caused by a Heterozygous Variant p.Cys326Phe in the SLC40A1 Gene and the Efficacy of Therapeutic Phlebotomy in Children

Published:2019-07 Issue:5 Volume:41 Page:e325-e328
ISSN:1077-4114
Container-title:Journal of Pediatric Hematology/Oncology
language:en
Short-container-title:

Author:

Shimura Masaru,Nishimata Shigeo,Saito Naoko,Tsutsumi Norito,Suzuki Shinji,Morishima Yasuyuki,Kashiwagi Yasuyo,Numabe Hironao,Kawashima Hisashi

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Oncology,Hematology,Pediatrics, Perinatology, and Child Health

Reference19 articles.

1. Global prevalence of putative haemochromatosis mutations;Merryweather-Clarke;J Med Gen,1997

2. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis;Feder;Nat Genet,1996

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

4. Human macrophage ferroportin biology and the basis for the ferroportin disease;Sabelli;Hepatology,2017

5. Hepcidin regulates cellular iron efflux by binding to ferroportin and inducing its internalization;Nemeth;Science,2004

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