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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...

詳細記述

保存先:
書誌詳細
主要な著者: Hanash, S. M., Rucknagel, D. L.
フォーマット: Artigo
言語:Inglês
出版事項: 1978
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC392790/
https://ncbi.nlm.nih.gov/pubmed/277945
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