Hb F-Emirates [Gγ59(E3)Lys→Glu] Observed in a Family of Sardinian Ancestry and Characterized by DNA Sequencing
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.1080/03630260500453990
Reference11 articles.
1. HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server
2. Two Fetal Hemoglobin Variants Affecting the Same Residue: HB F-Emirates [Gγ59(E3)LYS→GLU] and HB F-Sacromonte [Gγ59(E3)LYS→GLN]
3. Detection of the common Hb F Sardinia [Aγ(E19)Ile → Thr]variant by isoelectric focusing in normal newborns and in adults affected by elevated fetal hemoglobin syndromes
4. Globin Chain Electrophoresis: a New Approach to the Determination of theGγ/Aγ Ratio in Fetal Haemoglobin and to Studies of Globin Synthesis
5. The Gamma Globin Chain Heterogeneity of the Sardinian Newborn Baby
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1. Disorders of the synthesis of human fetal hemoglobin;IUBMB Life;2008
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