Use of Denaturing HPLC and a Heteroduplex Generator to Detect the HFE C282Y Mutation Associated with Genetic Hemochromatosis
Author:
Affiliation:
1. Unité de Physiopathologie Cellulaire et Moléculaire, CNRS UPR 2163, CHU Purpan, 31059 Toulouse Cedex 3, France
Publisher
Oxford University Press (OUP)
Subject
Biochemistry (medical),Clinical Biochemistry
Link
http://academic.oup.com/clinchem/article-pdf/49/5/822/32731747/clinchem0822.pdf
Reference20 articles.
1. A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis
2. Mutations in the MHC class I-like candidate gene for hemochromatosis in French patients
3. A Population-Based Study of the Clinical Expression of the Hemochromatosis Gene
4. Haemochromatosis and HLA–H
5. Haemochromatosis and HLA–H
Cited by 5 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. Hemochromatosis;Molecular Diagnostics;2010
2. Heteroduplex Analysis (HA);Encyclopedia of Medical Genomics and Proteomics;2004-12
3. Multiplex analysis of the most common mutations related to hereditary haemochromatosis: two methods combining specific amplification with capillary electrophoresis;European Journal of Haematology;2004-01-06
4. Integration of combined heteroduplex/restriction fragment length polymorphism analysis on an electrophoresis microchip for the detection of hereditary haemochromatosis;The Analyst;2004
5. Longevity and carrying the C282Y mutation for haemochromatosis on the HFE gene: case control study of 492 French centenarians;BMJ;2003-07-17
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