Hb S/β°-Thalassemia due to the ˜1.4-kb deletion is associated with a relatively mild phenotype
Author:
Publisher
Wiley
Subject
Hematology
Reference27 articles.
1. Clinical diversity of sickle cell anemia: Genetic and cellular modulation of disease severity
2. Hb S(C)-β+-thalassaemia: different mutations are associated with different levels of normal Hb A
3. Severe Hb S-β°-thalassaemia with a T → C substitution in the donor splice site of the first intron of the β-globin gene
4. Partial deletion of the 5' beta-globin gene region causes beta zero- thalassemia in members of an American black family
5. Molecular characterization of a beta zero-thalassemia resulting from a 1.4 kilobase deletion
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1. HbA 2 induction: the merit of pancellularity in sickle cell disease;British Journal of Haematology;2021-06
2. Whole genome sequence-based haplotypes reveal a single origin of the 1393 bp HBB deletion;Journal of Medical Genetics;2020-01-30
3. Characterization of Two Novel Deletions Involving the 5′ Region of the β-Globin Gene;Hemoglobin;2017-11-02
4. Diverse hematological phenotypes of β-thalassemia carriers;Annals of the New York Academy of Sciences;2016-03
5. HbA2: biology, clinical relevance and a possible target for ameliorating sickle cell disease;British Journal of Haematology;2015-06-24
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