Hemoglobin Hamadan or α2β256(D7)Gly→Arg in a Turkish Family
Author:
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630268408991728
Reference7 articles.
1. Haemoglobin Hamadan: α2A β2 56 (D7) glycine → arginine
2. Blouquit Y., Galacteros F., Arous N., Touboul A., Braconnier F., Riou J., Rosa J. Int. Cong. ISH-ISBT, Budapest August, 1982; 221, Abstract
3. Separation of Human Hemoglobins by Deae-Cellulose Chromatography using Glycine-Kcn-Nacl Developers
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1. A New Hemoglobin Variant: Hb Izmir [β86(F2)Ala→Val, GCC>GTC; HBB:c.260C>T];Hemoglobin;2012-06
2. Hemoglobin Q-Iran detected in family members from Northern Iran: a case report;Journal of Medical Case Reports;2012-02-06
3. Hb Leeds [β56(D7)Gly→Cys]: A New Hemoglobin that Aggravates Anemia in a child with β0-Thalassemia Trait;Hemoglobin;2007-01
4. First observation of homozygous hemoglobin hamadan (B 56 (D7) GLY-ARG) and beta thalassemia (-29 G>A)- hemoglobin Hamadan combination in a Turkish family;American Journal of Hematology;2003-11-17
5. Heterozygous hemoglobin Hamadan affects HbA1c assay.;Diabetes Care;1999-01-01
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