Hb Setif or α294(G1)Asp→Tyrβ2 Observed in a Saudi Arabian Family
Author:
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630268508996987
Reference13 articles.
1. Hb Setif: G1 (94)α Asp → Tyr a new α chain hemoglobin variant with substitution of the residue involved in a hydrogen bond between unlike subunits
2. Hemoglobin Setif (α94 (G1) ASP → TYR) in Iran a Report of 9 Cases
3. Hemoglobin setif and in vitro pseudosickling noted in a family with co-existent α and β thalassemia
4. Separation of Human Hemoglobins by Deae-Cellulose Chromatography using Glycine-Kcn-Nacl Developers
5. PROTEIN COAGULATION AND ITS REVERSAL
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1. Characterization of Homozygous Hb Setif (HBA2: c.283G>T) in the Iranian Population;Hemoglobin;2015-11-16
2. Molecular nature of alpha-globin genes in the Saudi population;Saudi Medical Journal;2015-11
3. Genetic Disorders in Saudi Arabia;Genetic Disorders Among Arab Populations;2010
4. Association of Mild and Severely Unstable α Chain Variants: The First Observation of a Compound Heterozygote with Hb Setif [α94(G1)Asp→Tyr (α2)] and Hb Agrinio [α29(B10)Leu→Pro (α2)] in a Greek Family;Hemoglobin;2008-01
5. Hb Jeddah [α68(E17)Asn→His (α1)]: A Newly Recognized α Chain Variant, Seen in Combination with Hb S [β6(A3)Glu→Val], and Found in Three Separate Families of Middle Eastern Origin;Hemoglobin;2008-01
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