Associated Papers
Case report: Curing a rare, unstable hemoglobin variant Hb Bristol-Alesha using haploidentical hematopoietic stem cell transplantation.
Zhang Q et al.
Frontiers in Immunology, 2023
Evaluation of in silico predictors on short nucleotide variants in HBA1, HBA2, and HBB associated with haemoglobinopathies.
Tamana S et al.
Elife, 2022
36453528 (PubMed )
Supplement: elife-79713-supp2.xlsx › Input-HBB
De novo HBB frameshift mutation in a patient with dominant β-thalassemia major.
Zhou X et al.
International Journal of Laboratory Hematology, 2022
The spectrum of beta-thalassemia mutations in the 22 Arab countries: a systematic review.
Khan AM et al.
Expert Review of Hematology, 2021
A Novel Human β-Globin Gene Variant [Hb London-Ontario, HBB: c.332T>G] is Associated with Transfusion-Dependent Anemia in a Patient with a Hemoglobin Electrophoresis Pattern Consistent with β-Thalassemia Trait.
Bienz MN et al.
Hemoglobin, 2019
Novel dominant β-thalassemia: Hb Boston-Kuwait [codon 139/140(+T)].
Croteau SE et al.
Pediatric Blood & Cancer, 2013
A De Novo Heterozygous Variant (HBB: c.379delG, p.Val127Cysfs*32) Associated with a Mild β-Thalassemia Intermedia Phenotype in a Turkish Child.
Gürlek-Gökçebay D et al.
Hemoglobin, 0
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