Targeted mutagenesis of the murine transferrin receptor-2 gene produces hemochromatosis

Hereditary hemochromatosis (HH) is a common genetic disorder characterized by excess absorption of dietary iron and progressive iron deposition in several tissues, particularly liver. The vast majority of individuals with HH are homozygous for mutations in the HFE gene. Recently a second transferrin...

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Détails bibliographiques
Auteurs principaux: Fleming, Robert E., Ahmann, John R., Migas, Mary C., Waheed, Abdul, Koeffler, H. Phillip, Kawabata, Hiroshi, Britton, Robert S., Bacon, Bruce R., Sly, William S.
Format: Artigo
Langue:Inglês
Publié: National Academy of Sciences 2002
Sujets:
Biological Sciences
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC125003/
https://ncbi.nlm.nih.gov/pubmed/12134060
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.162360699
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