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
Krüppel-Like Factor 1: A Pivotal Gene Regulator in Erythropoiesis.
Caria CA et al.
Cells, 2022
Compound Heterozygosity for KLF1 Mutations Causing Hemolytic Anemia in Children: A Case Report and Literature Review.
Xu L et al.
Frontiers in Genetics, 2021
The GenomeAsia 100K Project enables genetic discoveries across Asia.
Unknown Author
Nature, 2019
31802016 (PubMed )
Supplement: 41586_2019_1793_MOESM3_ESM.xlsx › S4b_-_Disease_Var
Variable serologic and other phenotypes due to KLF1 mutations.
Gillinder K et al.
Transfusion, 2018
An Unusual Hydrops Fetalis Associated with Compound Heterozygosity for Krüppel-like Factor 1 mutations.
Lee HH et al.
Hemoglobin, 2016
Can mutations in the gene encoding transcription factor EKLF (Erythroid Krüppel-Like Factor) protect us against infectious and parasitic diseases?
Mikołajczyk K et al.
Postepy Higieny I Medycyny Doswiadczalnej (online), 2016
Krüppeling erythropoiesis: an unexpected broad spectrum of human red blood cell disorders due to KLF1 variants.
Perkins A et al.
Blood, 2016
Compound heterozygosity for KLF1 mutations is associated with microcytic hypochromic anemia and increased fetal hemoglobin.
Huang J et al.
European Journal of Human Genetics : Ejhg, 2015
Changes in hematological parameters in α-thalassemia individuals co-inherited with erythroid Krüppel-like factor mutations.
Yu LH et al.
Clinical Genetics, 2015
Krüppel-like factor 1: hematologic phenotypes associated with KLF1 gene mutations.
Waye JS et al.
International Journal of Laboratory Hematology, 2015
Congenital Nonspherocytic Hemolytic Anemia Caused by Krüppel-Like Factor 1 Gene Variants: Another Case Report.
Jiang H et al.
Hemoglobin, 0
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