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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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Autors principals: Kan, Yuet Wai, Schwartz, Elias, Nathan, David G.
Format: Artigo
Idioma:Inglês
Publicat: 1968
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC297416/
https://ncbi.nlm.nih.gov/pubmed/5775343
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