Defect in messenger RNA for human hemoglobin synthesis in beta thalassemia
Functional messenger RNA for human hemoglobin synthesis was prepared from reticulocyte lysates of patients with homozygous beta thalassemia and sickle cell anemia. The messenger RNA stimulated the synthesis of human globin chains by a cell-free system derived from Krebs mouse ascites cells. In the p...
Guardat en:
| Publicat a: | J Clin Invest |
|---|---|
| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Society for Clinical Investigation
1971
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC292227/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/5129324/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI106778 |
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