A New Hemoglobin Variant: Hb Izmir [β86(F2)Ala→Val, GCC>GTC; HBB:c.260C>T]
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269.2012.717514
Reference14 articles.
1. Hemoglobin Hamadan or α2β256(D7)Gly→Arg in a Turkish Family
2. Hb Beograd-β° Thalassemia in a Turkish Family from Yugoslavia
3. Hb adana or α259(E8)Gly→Aspβ2, A severely unstable α1-globin variant, observed in combination with the -(α)20.5 KB α-thal-1 deletion in two Turkish patients
4. Compound Heterozygosity for HB E-Saskatoon or α2β222(B4)GLU→LYS and β-Thalassemia Type IVS-I-6 (T→C)
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1. Hb Wanjiang: A New β-Globin Chain Variant with Two Amino Acid Substitutions (HBB: c.255_264delinsTTTTTCTCAG);Hemoglobin;2022-03-04
2. Hb Belluno [β111(G13)Val→Gly;β133(H11)Val→Val (HBB: c.335T > G;402G > C)]: Incidental Detection of a New Clinically SilentβChain Variant During Hb A1cDetermination by High Performance Liquid Chromatography;Hemoglobin;2016-03-31
3. Molecular analysis of abnormal hemoglobins in beta chain in Aegean region of Turkey and first reports of hemoglobin Andrew-Minneapolis and Hb Hinsdale from Turkey;Hematology;2014-10-14
4. An Updated Review of Abnormal Hemoglobins in the Turkish Population;Turkish Journal of Hematology;2014-03-01
5. A Rare Hemoglobin Variant Which Interfered Hemoglobin A1C Result: Hemoglobin South Florida [β1(NA1)Val>Met, GTG>ATG; HBB: c.4G>A];Turkish Journal of Biochemistry;2014
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