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-Full_dataset
Hb Narges Lab, a Novel Hemoglobin Variant of the β-Globin Gene.
Hamid M et al.
Archives of Iranian Medicine, 2022
Multiplex minisequencing screen for common Southeast Asian and Indian beta-thalassemia mutations.
Wang W et al.
Clinical Chemistry, 2003
Molecular genetics of cystinuria: mutation analysis of SLC3A1 and evidence for another gene in type I (silent) phenotype.
Saadi I et al.
Kidney International, 1998
Expression studies of delta-globin gene alleles associated with reduced hemoglobin A2 levels in Greek Cypriots.
Trifillis P et al.
The Journal of Biological Chemistry, 1996
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