Associated Papers
Genetic Correlation of HBB, HFE and HAMP Genes to Endocrinal Complications in Egyptian Beta Thalassemia Major Patients.
Sokkar MF et al.
Biochemical Genetics, 2025
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
Curating the gnomAD database: Report of novel variants in the globin-coding genes and bioinformatics analysis.
Scheps KG et al.
Human Mutation, 2020
Human cleaving embryos enable robust homozygotic nucleotide substitutions by base editors.
Zhang M et al.
Genome Biology, 2019
[CYP2D6 and GSTM1 genetic polymorphism and lung cancer susceptibility].
Gao J et al.
Zhonghua Zhong Liu Za Zhi [chinese Journal of Oncology], 1998
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