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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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Bibliographic Details
Published in:Proc Natl Acad Sci U S A
Main Authors: Hanash, S. M., Rucknagel, D. L.
Format: Artigo
Language:Inglês
Published: National Academy of Sciences 1978
Subjects:
Online Access: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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