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Globin gene deletion in HPFH, δ°β° thalassaemia and Hb Lepore disease

✍ Scribed by OTTOLENGHI, S.; GIGLIONI, B.; COMI, P.; GIANNI, A. M.; POLLI, E.; ACQUAYE, C. T. A.; OLDHAM, J. H.; MASERA, G.


Book ID
109713680
Publisher
Nature Publishing Group
Year
1979
Tongue
English
Weight
518 KB
Volume
278
Category
Article
ISSN
0028-0836

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β-Globin gene haplotype in Hb SC disease
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We asked the question, is the haplotype found with the sickle hemoglobin gene associated with different hematological characteristics in patients who were combined heterozygotes for sickle hemoglobin and hemoglobin C (Hb SC disease)? In 73 adults with Hb SC disease, a Benin haplotype chromosome was