Homozygous State for Hb Constant Spring (Slow-moving Hb X Components)

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Molecular characterization of thalassemia intermedia with homozygous Hb Malay and Hb Malay/HbE in Thai patients.

Patients with thalassemia intermedia have a mild anemia and survive without needing regular blood transfusions.1 Here we report two cases of Thai patients with β-thalassemia intermedia caused by homozygosity of hemoglobin Malay (Hb Malay; α2β219Asn-Ser)2 and compound heterozygosity of Hb Malay and hemoglobin E (Hb E; α2β226Glu-Lys). Both patients presented with a history of anemia with marked m...

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ژورنال

عنوان ژورنال: Blood

سال: 1974

ISSN: 0006-4971,1528-0020

DOI: 10.1182/blood.v43.2.251.251