A carregar...

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,...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Raha-Chowdhury, R, Bowen, D J, Burnett, A K, Worwood, M
Formato: Artigo
Idioma:Inglês
Publicado em: 1995
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1050484/
https://ncbi.nlm.nih.gov/pubmed/7666396
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!