Associated Papers
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-HBA2
A Novel Mutation at HBA1: c.349G>T Causing α-Thalassemia in a Chinese Family.
Yin Z et al.
Hemoglobin, 2021
Hemoglobin Kirklareli (α H58L), a New Variant Associated with Iron Deficiency and Increased CO Binding.
Bissé E et al.
The Journal of Biological Chemistry, 2017
Molecular and Hematological Characterization of a Novel Translation Initiation Codon Mutation of the α2-Globin Gene (ATG>ATC or HBA2: c.3G>C).
Lei YL et al.
Hemoglobin, 0
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