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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...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
1968
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC297416/ https://ncbi.nlm.nih.gov/pubmed/5775343 |
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