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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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Main Authors: | , |
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Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
1978
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC392790/ https://ncbi.nlm.nih.gov/pubmed/277945 |
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