Hb A2/E levels found in co-inheritance with the α-thalassemia-1- SEA/ type deletion and either Hb e or β-thalassemia

• المؤلفون الرئيسيون: Pornprasert S., Treesuwan K., Punyamung M., Kongthai K.
• التنسيق: دورية
• منشور في: 2017
• الوصول للمادة أونلاين: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84862863861&origin=inward; http://cmuir.cmu.ac.th/jspui/handle/6653943832/42801
• المؤسسة: Chiang Mai University

The α-thalassemia-1 (α-thal-1) Southeast Asian ( SEA ) type deletion, β-thalassemia (β-thal) and Hb E [β26(B8)Glu→Lys, GAG > AAG] are the most common genetic disorders in Southeast Asian populations. Mean corpuscular volume (MCV) < 80.0 fL with normal hemoglobin (Hb) is used for screening α-...