A previously undescribed nonsense mutation of the HFE gene
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-0004.2002.610108.x/fullpdf
Reference14 articles.
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2. Heredity of idiopathic haemochromatosis: a study of 106 families;Simon;Clin Genet,1977
3. The effect of HFE genotypes in patients attending a health appraisal clinic;Beutler;Ann Intern Med,2000
4. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis;Feder;Nature Genet,1996
5. Spectrum of mutations in the HFE gene implicated in haemochromatosis and porphyria;De Villiers;Hum Mol Genet,1999
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2. Transient elevation of serum ferritin in a Sri Lankan with homozygosity for H63D mutation in the HFE gene: a case report;Journal of Medical Case Reports;2020-07-09
3. HFE-Related Hemochromatosis in a Chinese Patient: The First Reported Case;Frontiers in Genetics;2020-02-21
4. A novel homozygous stop-codon mutation in human HFE responsible for nonsense-mediated mRNA decay;Blood Cells, Molecules, and Diseases;2014-09
5. Mutations in the HFE, TFR2, and SLC40A1 genes in patients with hemochromatosis;Gene;2012-10
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