Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results
Authors:
- 1 November 1999
- journal article
- other
- Published by Springer Nature in Nature Genetics
- Vol. 23 (3) , 271
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- An HFE Intronic Variant Promotes Misdiagnosis of Hereditary HemochromatosisThe American Journal of Human Genetics, 1999
- Polymorphism in intron 4 of HFE may cause overestimation of C282Y homozygote prevalence in haemochromatosisNature Genetics, 1999
- Rapid Detection of Genetic Mutations Associated with HaemochromatosisVox Sanguinis, 1998
- Heterogeneity of hemochromatosis in Italy☆☆☆Gastroenterology, 1998
- A simple genetic test identifies 90% of UK patients with haemochromatosisGut, 1997
- Hereditary hemochromatosis: aHpal polymorphism within the HLA-H geneMolecular and Cellular Probes, 1997
- Global prevalence of putative haemochromatosis mutations.Journal of Medical Genetics, 1997
- Mutations in the MHC class I-like candidate gene for hemochromatosis in French patientsImmunogenetics, 1997
- Haemochromatosis and HLA–HNature Genetics, 1996
- A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosisNature Genetics, 1996