Masking of a β-Thalassemia Determinant by a Novel δ-Globin Gene Defect [Hb A2-Saurashtra or δ100(G2)Pro→Ser;HBD: c.301C>T] inCis
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269.2013.852568
Reference15 articles.
1. Frequency of β-thalassemia trait and other hemoglobinopathies in northern and western India
2. Editorial: Measurement of HbA2
3. Clinical heterogeneity of silent-gene B-thalassemia among Indians
4. Occurrence of common and rare δ-globin gene defects in two multiethnic populations: thirteen new mutations and the significance of δ-globin gene defects in β-thalassemia diagnostics
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2. Unresolved laboratory issues of the heterozygous state of β-thalassemia: a literature review;Haematologica;2023-06-01
3. Significance of borderline HbA2 levels in β thalassemia carrier screening;Scientific Reports;2022-03-30
4. A New Mutation, Hb A2-Canakkale [δ10(A7)Ala→Val; HBD: c.32C>T], and Other Well-Known δ Variants Identified in a Selected Cohort with Low Hb A2 Levels;Hemoglobin;2022-03-04
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