Hb E and α-Thalassemia; Variability in the Assembly of βEChain Containing Tetramers
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269708997383
Reference27 articles.
1. Trimodality in Tie Percentages of β Chain Variants in Heterozy-Gotes: The Effect of the Number of Aczive HBαStructural Loci
2. Percentages of abnormal hemoglobins in adults with a heterozygosity for an α-chain and/or a β-chain variant
3. Differences in Affinity of Variant β Chains for a Chains: A Possible Explanation for the Variation in the Percentages of β Chain Variants in Heterozygotes
4. Competition of normal β chains and sickle haemoglobin β chains for α chains as a post-translational control mechanism
5. Electrostatic interactions in the assembly of haemoglobin
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2. The Hb E (HBB: c.79G>A), Mean Corpuscular Volume, Mean Corpuscular Hemoglobin Cutoff Points in Double Heterozygous Hb E/– –SEAα-Thalassemia-1 Carriers are Dependent on Hemoglobin Levels;Hemoglobin;2017-01-02
3. Problems in determining thalassemia carrier status in a program for prevention and control of severe thalassemia syndromes: a lesson from Thailand;Clinical Chemistry and Laboratory Medicine (CCLM);2013-03-23
4. Hemoglobin Variants: Biochemical Properties and Clinical Correlates;Cold Spring Harbor Perspectives in Medicine;2013-02-06
5. Complex Interaction of Hb E [β26(B8)Glu→Lys], Hb Korle-Bu [β73(E17)Asp→Asn] and a Deletional α-thalassemia-1 in Pregnancy;Hemoglobin;2009-12
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