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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Bibliografiske detaljer

Udgivet i:	J Clin Invest
Principais autores:	Kan, Yuet Wai, Schwartz, Elias, Nathan, David G.
Format:	Artigo
Sprog:	Inglês
Udgivet:	American Society for Clinical Investigation 1968
Fag:	Articles
Online adgang:	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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