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...
Αποθηκεύτηκε σε:
| Εκδόθηκε σε: | J Clin Invest |
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| Κύριοι συγγραφείς: | , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
American Society for Clinical Investigation
1968
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC297416/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/5775343/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI105933 |
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