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Synthesis of Globin Chains in Sickle β-Thalassemia

In five patients with sickle β-thalassemia there was balanced α- and β-globin synthesis in the bone marrow and decreased total β-chain synthesis relative to that of α-chain in the peripheral blood. These findings are similar to those in patients with simple β-thalassemia trait. Despite a range of he...

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Dettagli Bibliografici
Autori principali: Gill, Frances M., Schwartz, Elias
Natura: Artigo
Lingua:Inglês
Pubblicazione: 1973
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC302309/
https://ncbi.nlm.nih.gov/pubmed/4685090
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