Allelic associations and homozygosity at loci from HLA-B to D6S299 in genetic haemochromatosis.

Haemochromatosis (GH) is an autosomal recessive disorder in which increased iron absorption causes iron overload. The gene (HFE) is closely linked to HLA-A on chromosome 6 (6p21.3) but has not yet been identified. We have examined eight polymorphic loci, HLA-B (most centromeric), I82, D6S265, HLA-A,...

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Main Authors: Raha-Chowdhury, R, Bowen, D J, Burnett, A K, Worwood, M
Format: Artigo
Sprog:Inglês
Udgivet: 1995
Fag:
Research Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1050484/
https://ncbi.nlm.nih.gov/pubmed/7666396
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