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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Detalhes bibliográficos
Main Authors: 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.
Formato: Artigo
Idioma:en
Publicado em: National Academy of Sciences 2002
Assuntos:
Biological Sciences
Acesso em linha: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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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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