Hb A2/E levels found in co-inheritance with the α-thalassemia-1- SEA/ type deletion and either Hb e or β-thalassemia
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- and β-...
Saved in:
Main Authors: | Sakorn Pornprasert, Kallayanee Treesuwan, Manoo Punyamung, Kunyakan Kongthai |
---|---|
Format: | Journal |
Published: |
2018
|
Subjects: | |
Online Access: | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84862863861&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/51367 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Chiang Mai University |
Similar Items
-
Hb A2/E levels found in co-inheritance with the α-thalassemia-1- SEA/ type deletion and either Hb e or β-thalassemia
by: Pornprasert S., et al.
Published: (2017) -
A formula to identify potential cases of β-thalassemia/HbE disease among patients with absent HbA, HbE >75% and HbF between 5 and 15%
by: Sakorn Pornprasert, et al.
Published: (2019) -
Comparison of capillary electrophoregram among heterozygous Hb Hope, Hb Hope/α-thalassemia-1 SEA type deletion and Hb Hope/β0- thalassemia
by: Sakorn Pornprasert, et al.
Published: (2018) -
Criteria for detection of α-Thalassemia-1 Thai type deletion in routine laboratory
by: Sakorn Pornprasert, et al.
Published: (2018) -
Criteria for detection of α-Thalassemia-1 Thai type deletion in routine laboratory
by: Sakorn Pornprasert, et al.
Published: (2018)