Homozygous mutation of the 5'UTR region of the L-Ferritin gene in the hereditary hyperferritinemia cataract syndrome and its impact on the phenotype-Reference-Cited by-同舟云学术

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Homozygous mutation of the 5'UTR region of the L-Ferritin gene in the hereditary hyperferritinemia cataract syndrome and its impact on the phenotype

Published:2013-01-08 Issue:4 Volume:98 Page:e42-e43
ISSN:0390-6078
Container-title:Haematologica
language:en
Short-container-title:Haematologica

Author:

Giansily-Blaizot M.,Cunat S.,Moulis G.,Schved J.-F.,Aguilar-Martinez P.

Publisher

Ferrata Storti Foundation (Haematologica)

Subject

Hematology

Cited by 10 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 iron matters: Aged microplastics disrupted the iron homeostasis in the liver organoids;Science of The Total Environment;2024-01

2. Hereditary Hyperferritinemia-Cataract Syndrome in a Family With HFE-H63D Mutation;Cureus;2023-03-16

3. Cataract;Clinical Ophthalmic Genetics and Genomics;2022

4. Hereditary Hyperferritinemia Cataract Syndrome: Ferritin L Gene and Physiopathology behind the Disease—Report of New Cases;International Journal of Molecular Sciences;2021-05-21

5. Iron Metabolism and Related Disorders;Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics;2021

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