De novo initiation codon mutation (ATG→ACG) of the β-globin gene causing β-thalassemia in a swiss family
Author:
Publisher
Wiley
Subject
Hematology
Reference24 articles.
1. An initiation codon mutation (AUG----GUG) of the human alpha 1-globin gene. Structural characterization and evidence for a mild thalassemic phenotype.
2. Initiation codon mutation as a cause of alpha thalassemia.
3. An alpha-globin gene initiation codon mutation in a black family with HbH disease
4. HOMOZYGOUS NON-DELETION α2GLOBIN GENE MUTATION (INITIATION CODON MUTATION): CLINICAL AND HAEMATOLOGICAL PHENOTYPE
5. An Initiation Codon Mutation as a Cause of a β-Thalassemia
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1. Detection of a Rare Mutation in the Initiation Codon of the β-Globin Gene (HBB:C.2T > C; P.Met1Thr);Hemoglobin;2023-05-04
2. Case Report: β-thalassemia major on the East African coast;Wellcome Open Research;2022-07-13
3. β‐Thalassemia pathogenic variants in a cohort of children from the East African coast;Molecular Genetics & Genomic Medicine;2020-05-11
4. A Novel Pathogenic β-Thalassemia Mutation Identified at Codon 8 (HBB: c.27delG) in a Bangladeshi Family AcquiredDe Novo;Hemoglobin;2019-05-04
5. Rare β- and δ-Globin Gene Mutations in the Pathare Prabhus: Original Inhabitants of Mumbai, India;Hemoglobin;2018-11-02
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