HB Sögn or α2β214(A11)LEU → ARG in Combination with an α-Thalassemia Heterozygosity
Author:
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269609027918
Reference11 articles.
1. Haemoglobin Sogn (β14 Arginine) A New Haemoglobin Variant
2. Hb Sogn (β14 Arginine)
3. Two Families With Hemoglobin Sogn, β(A11)14 Leu→Arg, in Minnesota and Indiana: Hematologic, Functional, and Biosynthetic Features
4. Heterozygosity for the IVS-I-5(G→C) mutation with a G→A change at codon 18 (Val→Met; Hb Baden) in cis and a T→G mutation at codon 126 (Val→Gly; Hb Djonburi) in trans resulting in a thalassemia intermedia
5. HB Alesha or α2β267(E11)VAL →MET: A New Unstable Hemoglobin Variant Identified Through Sequencing of, Amplified DNA
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