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...
Gardado en:
| Publicado en: | J Clin Invest |
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| Principais autores: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
American Society for Clinical Investigation
1971
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| Assuntos: | |
| Acceso en liña: | 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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