Concurrent sickle cell anemia and alpha-thalassemia. Effect on pathological properties of sickle erythrocytes.

The concurrence of sickle cell anemia and alpha-thalassemia results in less severe hemolytic anemia apparently as a result of reduced intraerythrocytic concentration of hemoglobin S and its retarded polymerization. We have evaluated the effect of alpha-globin gene number on several interrelated prop...

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Vydáno v:	J Clin Invest
Hlavní autoři:	Embury, S H, Clark, M R, Monroy, G, Mohandas, N
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	American Society for Clinical Investigation 1984
Témata:	Research Article
On-line přístup:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC424978/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6690472/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI111181
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