Associated Papers
Molecular and haematological characterisation of haemolytic anaemia associated with biallelic KLF1 mutations: a case series.
Singha K et al.
Journal of Clinical Pathology, 2024
Compound Heterozygosity for KLF1 Mutations Causing Hemolytic Anemia in Children: A Case Report and Literature Review.
Xu L et al.
Frontiers in Genetics, 2021
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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