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Detection of Hb Constant Spring [ α142, Term→Gln, TAA> CAA ( α2)] in Heterozygotes Combined With β-Thalassemia.

Authors :
Li, You-Qiong
Li, Ru
Li, Dong-Zhi
Source :
Hemoglobin. Apr2013, Vol. 37 Issue 2, p197-200. 4p.
Publication Year :
2013

Abstract

Hb Constant Spring [Hb CS, α142, Term→Gln, TAA>CAA (α2)] is a nondeletional form of α-thalassemia (α-thal) that is most prevalent in Southern Chinese and Southeast Asian populations. We previously found that Hb CS trait could efficiently be screened using Sebia Capillarys2. In this study, we report that Hb CS heterozygotes combined with β-thal could not be detected by the Sebia Capillarys2 method due to the very small amount of Hb CS. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03630269
Volume :
37
Issue :
2
Database :
Academic Search Index
Journal :
Hemoglobin
Publication Type :
Academic Journal
Accession number :
85938297
Full Text :
https://doi.org/10.3109/03630269.2013.768532