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How mutant HFE causes hereditary hemochromatosis
In this issue of Blood, Wu et al describe the molecular function of HFE, the gene most commonly mutated in hereditary hemochromatosis (HH).(1) HH is the most frequent genetic disorder of the Western world. The authors show that HFE prevents ubiquitination and proteasomal degradation of bone-morphoge...
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| Hlavní autor: | |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
American Society of Hematology
2014
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4141508/ https://ncbi.nlm.nih.gov/pubmed/25147378 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2014-07-581744 |
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