Associated Papers
Targeted next-generation sequencing and long-read HiFi sequencing provide novel insights into clinically significant KLF1 variants.
Ye L et al.
Bmc Genomics, 2024
Identification of Lutheran Blood Groups and Genetic Variants within KLF1 among Thai Blood Donors.
Intharanut K et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2023
Novel variants in Krueppel like factor 1 that cause persistence of fetal hemoglobin in In(Lu) individuals.
Eernstman J et al.
Scientific Reports, 2021
Identifying genetic variants and pathways associated with extreme levels of fetal hemoglobin in sickle cell disease in Tanzania.
Nkya S et al.
Bmc Medical Genetics, 2020
32503527 (PubMed )
Supplement: 12881_2020_1059_MOESM2_ESM.xlsx › Sheet1
Mutations of the KLF1 gene detected in Japanese with the In(Lu) phenotype.
Kawai M et al.
Transfusion, 2017
Select a paper to view details