Global prevalence of putative haemochromatosis mutations.

Haemochromatosis is a genetic disease associated with progressive iron overload, and is common among populations of northern European origin. HLA-H is a recently reported candidate gene for this condition. Two mutations have been identified, a substitution of cysteine for tyrosine at amino acid 282...

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Bibliografiske detaljer
Main Authors: Merryweather-Clarke, A T, Pointon, J J, Shearman, J D, Robson, K J
Format: Artigo
Sprog:Inglês
Udgivet: 1997
Fag:
Research Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1050911/
https://ncbi.nlm.nih.gov/pubmed/9138148
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