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Erythrocyte δ-aminolevulinic acid dehydrase activity in thalassemia major and sickle-cell anemia

✍ Scribed by Felix Feldman; Herbert C. Lichtman


Book ID
115791463
Publisher
Elsevier Science
Year
1962
Weight
177 KB
Volume
58
Category
Article
ISSN
0006-3002

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We have analyzed the hemoglobin abnormalities in nearly 50 Albanian patients with a significant hemoglobinopathy and included 37 relatives in this study. Sickle cell anemia (SS) is a common disorder; all 15 sickle cell anemia patients had the complications expected for this disease. The beta S haplo