KLF1Gene Mutations in Chinese Adults with Increased Fetal Hemoglobin
Author:
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269.2013.805304
Reference15 articles.
1. The multifunctional role of EKLF/KLF1 during erythropoiesis
2. Mutations in EKLF/KLF1 form the molecular basis of the rare blood group In(Lu) phenotype
3. Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin
4. Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrin
5. A Dominant Mutation in the Gene Encoding the Erythroid Transcription Factor KLF1 Causes a Congenital Dyserythropoietic Anemia
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1. Severe neonatal haemolytic anaemia caused by compound heterozygous KLF1 mutations: report of four families and literature review;British Journal of Haematology;2021-07-05
2. Epigenetic Insights and Potential Modifiers as Therapeutic Targets in β–Thalassemia;Biomolecules;2021-05-18
3. Thalassemia and erythroid transcription factor KLF1 mutations associated with borderline hemoglobin A2 in the Thai population;Archives of Medical Science;2020-08-11
4. Differential role of Kruppel like factor 1 (KLF1) gene in red blood cell disorders;Genomics;2019-12
5. Alterations on high HbF levels may be associated with KLF1 gene mutations;Cellular and Molecular Biology;2017-08-30
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