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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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Detaylı Bibliyografya
Asıl Yazarlar: Embury, S H, Clark, M R, Monroy, G, Mohandas, N
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1984
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC424978/
https://ncbi.nlm.nih.gov/pubmed/6690472
Etiketler: Etiketle
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