Elevated Hb A2Levels in a Patient with a Compound Heterozygosity for the(β+) −31 (A > G) and (β0) Codon 17 (A > T) Mutations Together with a Singleα-Globin Gene
Author:
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269.2015.1047513
Reference19 articles.
1. SYTO9 and SYBR Green1 with High Resolution Melting Analysis for Molecular Confirmatory Testing of the Common Southeast Asian β0-thalassemia Mutations
2. Detection of β-Thalassemia Mutations Using a Multiplex Amplification Refractory Mutation System Assay
3. Severity differences in β-thalassaemia/haemoglobin E syndromes: implication of genetic factors
4. β-Thalassemia Intermedia with Exceptionally High Hemoglobin A2: Relationship to Mutations in the β-Gene Promoter
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1. Impact of α-Globin Gene Expression and α-Globin Modifiers on the Phenotype of β-Thalassemia and Other Hemoglobinopathies: Implications for Patient Management;International Journal of Molecular Sciences;2024-03-17
2. Identification of two novel β-globin gene mutations HBB: exon3del, HBB: c.−81A>C;Hematology;2023-10-10
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