Associated Papers
Hematopoietic cell transplantation for congenital dyserythropoietic anemia IV caused by compound heterozygous KLF1 mutations.
Yang K et al.
Annals of Hematology, 2023
RBCeq: A robust and scalable algorithm for accurate genetic blood typing.
Jadhao S et al.
Ebiomedicine, 2022
35033986 (PubMed )
Supplement: mmc2.xlsx › Supplementary_Table11
Severe neonatal haemolytic anaemia caused by compound heterozygous KLF1 mutations: report of four families and literature review.
Tangsricharoen T et al.
British Journal of Haematology, 2021
Compound Heterozygosity for KLF1 Mutations Causing Hemolytic Anemia in Children: A Case Report and Literature Review.
Xu L et al.
Frontiers in Genetics, 2021
A Case of Hereditary Spherocytosis Caused by a Novel Homozygous Mutation in the SPTB Gene Misdiagnosed as β-Thalassemia Intermedia Due to a KLF1 Gene Mutation.
Yang K et al.
Hemoglobin, 2019
Molecular characterization and integrative genomic analysis of a panel of newly established penile cancer cell lines.
Zhou QH et al.
Cell Death & Disease, 2018
29880898 (PubMed )
Supplement: 41419_2018_736_MOESM7_ESM.xlsx › Sheet1
Analysis of the Genotypes in a Chinese Population with Increased Hb A2 and Low Hematological Indices.
Jiang F et al.
Hemoglobin, 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
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
Krüppel-like factor 1: hematologic phenotypes associated with KLF1 gene mutations.
Waye JS et al.
International Journal of Laboratory Hematology, 2015
Delineation of the molecular basis of borderline hemoglobin A2 in Chinese individuals.
Lou JW et al.
Blood Cells, Molecules & Diseases, 2014
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