An HFE Intronic Variant Promotes Misdiagnosis of Hereditary Hemochromatosis
- 1 September 1999
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 65 (3) , 924-926
- https://doi.org/10.1086/302550
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
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- Clinical and Biochemical Abnormalities in People Heterozygous for HemochromatosisNew England Journal of Medicine, 1996
- Haemochromatosis and HLA–HNature Genetics, 1996
- A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosisNature Genetics, 1996