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...
সংরক্ষণ করুন:
| প্রকাশিত: | Proc Natl Acad Sci U S A |
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| প্রধান লেখক: | , , , , , , , |
| বিন্যাস: | Artigo |
| ভাষা: | Inglês |
| প্রকাশিত: |
National Academy of Sciences
1997
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| বিষয়গুলি: | |
| অনলাইন ব্যবহার করুন: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC24286/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9371823/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.94.24.13198 |
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