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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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| Hovedforfatter: | |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
American Society of Hematology
2014
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| Fag: | |
| Online adgang: | 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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