Associated Papers
Gardos channelopathies: novel insights into KCNN4 mutations and their clinical impact.
Warang P et al.
Journal of Human Genetics, 2026
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
Rare cause of transfusion-dependent hemolytic anemia: A case report of HbE/Hb Nottingham and literature review.
Aziz A et al.
Pediatric Blood & Cancer, 2022
Genetic Analysis of the Salmonella FliE Protein That Forms the Base of the Flagellar Axial Structure.
Hendriksen JJ et al.
Mbio, 2021
Predictive SNPs for β0-thalassemia/HbE disease severity.
Munkongdee T et al.
Scientific Reports, 2021
33990643 (PubMed )
Supplement: 41598_2021_89641_MOESM1_ESM.pdf
Mild α-Thalassemia Caused by a Mosaic α-Globin Gene Mutation.
Wang RY et al.
Hemoglobin, 2021
A Naturally Occurring Deletion in FliE from Salmonella enterica Serovar Dublin Results in an Aflagellate Phenotype and Defective Proinflammatory Properties.
Sasías S et al.
Infection and Immunity, 2018
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