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Contributions of β2-microglobulin–dependent molecules and lymphocytes to iron regulation: insights from HfeRag1(−/−) and β2mRag1(−/−) double knock-out mice
Genetic causes of hereditary hemochromatosis (HH) include mutations in the HFE gene, coding for a β2-microglobulin (β2m)–associated major histocompatibility complex class I-like protein. However, iron accumulation in patients with HH can be highly variable. Previously, analysis of β2mRag1(−/−) doubl...
Bewaard in:
| Hoofdauteurs: | , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2003
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2891006/ https://ncbi.nlm.nih.gov/pubmed/14656877 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2003-09-3300 |
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