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Variable phenotypic presentation of iron overload in H63D homozygotes: are genetic modifiers the cause?
BACKGROUND—First considered as a polymorphism of the HFE gene, the H63D mutation is now widely recognised as a haemochromatosis associated allele. But few H63D homozygotes with clinical manifestations of hereditary haemochromatosis (HH) have been reported. Concurrently, an increasing number of genes...
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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2001
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1728323/ https://ncbi.nlm.nih.gov/pubmed/11358905 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/gut.48.6.836 |
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