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Lack of association of G779A ZHX-2 gene variant with HbF levels in β-thalassemia major

✍ Scribed by Anjana Munshi; Sneha Dadheech; Suman Jain; James Joseph; Amal Al-Hazzani; Ali A. Alshatwi; Mallemoggala Sai Babu; Koppula Rajeshwar; Akka Jyothy


Book ID
114794937
Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
85 KB
Volume
86
Category
Article
ISSN
0902-4441

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✍ Tadmouri, G. O.; Yüksel, L.; Başak, A. N. 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 36 KB 👁 1 views

␤-thalassemia and sickle cell disease (SCD) are common disorders in Turkey. Compound heterozygosity for these two disorders (␤ S /␤-thalassemia) is encountered frequently. In this report we present hematological and molecular data of two Turkish siblings with ␤ S /␤ del -thalassemia caused by a 290