Multicentric origin of hemochromatosis gene (HFE) mutations.

Genetic hemochromatosis (GH) is believed to be a disease restricted to those of European ancestry. In northwestern Europe, >80% of GH patients are homozygous for one mutation, the substitution of tyrosine for cysteine at position 282 (C282Y) in the unprocessed protein. In a proportion of GH patie...

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Sparad:
Bibliografiska uppgifter
Huvudupphovsmän: Rochette, J, Pointon, J J, Fisher, C A, Perera, G, Arambepola, M, Arichchi, D S, De Silva, S, Vandwalle, J L, Monti, J P, Old, J M, Merryweather-Clarke, A T, Weatherall, D J, Robson, K J
Materialtyp: Artigo
Språk:Inglês
Publicerad: 1999
Ämnen:
Research Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377829/
https://ncbi.nlm.nih.gov/pubmed/10090890
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