Associated Papers
Novel variants in Krueppel like factor 1 that cause persistence of fetal hemoglobin in In(Lu) individuals.
Eernstman J et al.
Scientific Reports, 2021
34535703 (PubMed )
Supplement: 41598_2021_97149_MOESM1_ESM.pdf
Nine known and five novel mutations in the erythroid transcription factor KLF1 gene and phenotypic expression of fetal hemoglobin in hemoglobin E disorder.
Tepakhan W et al.
Blood Cells, Molecules & Diseases, 2016
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