Detection of C282Y and H63D in theHFEGene
Author:
Affiliation:
1. MRC Molecular Haematology Unit, Institute Molecular Medicine, Headington, Oxford, OX3 9DS, UK.
2. Medical Genetics Service, Baschirotto Institute for Rare Disease, Europe, I-36023 Costozza di Longare (VI), Italy.
Publisher
Mary Ann Liebert Inc
Subject
Genetics (clinical)
Link
http://www.liebertpub.com/doi/pdf/10.1089/10906570050114803
Reference59 articles.
1. Rapid diagnosis of asymptomatic hereditary haemochromatosis by detection of the Cys282Tyr mutation in the HLA-H gene.
2. Genetic and Clinical Description of Hemochromatosis Probands and Heterozygotes: Evidence That Multiple Genes Linked to the Major Histocompatibility Complex Are Responsible for Hemochromatosis
3. Development of a multiplex ARMS test for mutations in the HFE gene associated with hereditary haemochromatosis
4. Homogeneous Multiplex Genotyping of Hemochromatosis Mutations with Fluorescent Hybridization Probes
5. The Significance of the 187G (H63D) Mutation in Hemochromatosis
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