Proteolytic activity in erythrocyte precursors
Thalassemia is characterized by unequal rates of synthesis of the α and β globin chains that are part of the hemoglobin tetramer. In the type of thalassemia due to a defect in β-chain synthesis (β-thalassemia), this imbalance results in a relative exoess of α-chains. We have studied the susceptibili...
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| Publicat a: | Proc Natl Acad Sci U S A |
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| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
National Academy of Sciences
1978
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC392790/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/277945/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.75.7.3427 |
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