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...
Uloženo v:
| Vydáno v: | J Clin Invest |
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| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
American Society for Clinical Investigation
1973
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC302309/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/4685090/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI107232 |
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