Structural and functional studies of hemoglobin J calabria: β64 (E8) Gly → Asp
Author:
Publisher
Elsevier BV
Subject
Biochemistry, Genetics and Molecular Biology (miscellaneous)
Reference29 articles.
1. Hereditary Heinz-Body Anaemia.
2. Structural studies of hemoglobin Saint Etienne β 92 (F8) his → GLN: A new abnormal hemoglobin with loss of β proximal histidine and absence of heme on the β chains
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1. Early Onset of Severe Anemia Caused by Hb Calgary ( HBB : C.194G > T): Another Case Report;Hemoglobin;2024-02-12
2. Hb Calgary (HBB: c.194G>T): A Highly Unstable Hemoglobin Variant with a β-Thalassemia Major Phenotype;Hemoglobin;2021-07-04
3. Hb F-Wentzville [Gγ24(B6)Gly→Glu; HBG2: c.74G>A, p.Gly25Glu]: An Unstable Gγ-Globin Variant Associated with Neonatal Hemolytic Anemia;Hemoglobin;2020-01-02
4. A new unstable variant of the fetal hemoglobinHBG2gene: Hb F-Turritana [Gγ64(E8)Gly→Asp, HBG2:c.194G>A] foundin cisto the Hb F-Sardinia gene [Aγ(E19)Ile→Thr, HBG1:c.227T>C];European Journal of Haematology;2014-02-26
5. Hb Extremadura [β64(E8)Gly→Ser;β133(H11)Val→Leu]: A New Molecular Analysis;Hemoglobin;2011-07-28
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