Compound Heterozygosity for HB E-Saskatoon or α2β222(B4)GLU→LYS and β-Thalassemia Type IVS-I-6 (T→C)
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269009032006
Reference5 articles.
1. Pathology of Abnormal Hemoglobin Diseases Seen in Thailand
2. Hb E and Hb E-Like Variants in Individuals from Turkey
3. Abnormal RNA processing due to the exon mutation of βE-globin gene
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1. High Frequency of Hb E-Saskatoon (HBB: c.67G > A) in Brazilians: A New Genetic Origin?;Hemoglobin;2016-06-02
2. A New Hemoglobin Variant: Hb Izmir [β86(F2)Ala→Val, GCC>GTC; HBB:c.260C>T];Hemoglobin;2012-06
3. Two rare hemoglobin variants in the Cukurova Region of Turkey: Hb E-Saskatoon and Hb G-Coushatta;Turkish Journal of Hematology;2011-12-01
4. The First Case of Hb E-Saskatoon Associated with Hb Lepore-Baltimore Found in Spain;Hemoglobin;2005-01
5. HOMOZYGOSITY FOR Hb E-SASKATOON [β22(B4)Glu → Lys] IN A TURKISH PATIENT;Hemoglobin;2001-01
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