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Globin chain synthesis in the alpha thalassemia syndromes
Whole blood samples of patients with various forms of alpha thalassemia including hemoglobin H disease, alpha thalassemia trait, and the “silent carrier” state were incubated with leucine-(14)C for definition of relative rates of production of alpha and beta chains in these disorders. The chains wer...
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| Главные авторы: | , , |
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| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
1968
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC297416/ https://ncbi.nlm.nih.gov/pubmed/5775343 |
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