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Association of the transferrin receptor in human placenta with HFE, the protein defective in hereditary hemochromatosis
Hereditary hemochromatosis (HH) is a common autosomal recessive disease associated with loss of regulation of dietary iron absorption and excessive iron deposition in major organs of the body. Recently, a candidate gene for HH (also called HFE) was identified that encodes a novel MHC class I-like pr...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | en |
| Publicado: |
The National Academy of Sciences of the USA
1997
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC24286/ https://ncbi.nlm.nih.gov/pubmed/9371823 |
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