The SLC40A1 R178Q mutation is a recurrent cause of hemochromatosis and is associated with a novel pathogenic mechanism-Reference-Cited by-同舟云学术

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The SLC40A1 R178Q mutation is a recurrent cause of hemochromatosis and is associated with a novel pathogenic mechanism

Published:2018-07-12 Issue:11 Volume:103 Page:1796-1805
ISSN:0390-6078
Container-title:Haematologica
language:en
Short-container-title:Haematologica

Author:

Ka Chandran,Guellec Julie,Pepermans Xavier,Kannengiesser Caroline,Ged Cécile,Wuyts Wim,Cassiman David,de Ledinghen Victor,Varet Bruno,de Kerguenec Caroline,Oudin Claire,Gourlaouen Isabelle,Lefebvre Thibaud,Férec Claude,Callebaut Isabelle,Le Gac Gérald

Publisher

Ferrata Storti Foundation (Haematologica)

Subject

Hematology

Cited by 22 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. The dual loss and gain of function of the FPN1 iron exporter results in the ferroportin disease phenotype;Human Genetics and Genomics Advances;2024-10

2. Insights into the role of glycerophospholipids on the iron export function of SLC40A1 and the molecular mechanisms of ferroportin disease;The FASEB Journal;2024-07-03

3. Hereditary haemochromatosis: Prevalence and characterization of the disease in a tertiary hospital in Aragon;Medicina Clínica;2024-07

4. Insights into the role of glycerophospholipids on the iron export function of SLC40A1 and the molecular mechanisms of ferroportin disease;2024-02-05

5. Cholesterol modulates the human FPN1 iron export function in plasma membrane liquid-ordered microdomains;2023-12-14

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