Hematopoietic cell transplantation for congenital dyserythropoietic anemia IV caused by compound heterozygous KLF1 mutations
Author:
Funder
the Key Science and Technology Project of Zigong
Publisher
Springer Science and Business Media LLC
Subject
Hematology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00277-023-05175-9.pdf
Reference18 articles.
1. Siatecka M, Bieker JJ (2011) The multifunctional role of EKLF/KLF1 during erythropoiesis. Blood 118:2044–2054. https://doi.org/10.1182/blood-2011-03-331371
2. Perkins A, Xu X, Higgs DR, Patrinos GP, Arnaud L, Bieker JJ, Philipsen S (2016) Krüppeling erythropoiesis: an unexpected broad spectrum of human red blood cell disorders due to KLF1 variants. Blood 127:1856–1862. https://doi.org/10.1182/blood-2016-01-694331
3. Xu L, Zhu D, Zhang Y, Liang G, Liang M, Wei X, Feng X, Wu X, Shang X (2021) Compound heterozygosity for KLF1 mutations causing hemolytic anemia in children: a case report and literature review. Front Genet 12:691461. https://doi.org/10.3389/fgene.2021.691461
4. Viprakasit V, Ekwattanakit S, Riolueang S, Chalaow N, Fisher C, Lower K, Kanno H, Tachavanich K, Bejrachandra S, Saipin J, Juntharaniyom M, Sanpakit K, Tanphaichitr VS, Songdej D, Babbs C, Gibbons RJ, Philipsen S, Higgs DR (2014) Mutations in Kruppel-like factor 1 cause transfusion-dependent hemolytic anemia and persistence of embryonic globin gene expression. Blood 123:1586–1595. https://doi.org/10.1182/blood-2013-09-526087
5. Belgemen-Ozer T, Gorukmez O (2020) A very rare congenital dyserythropoietic anemia variant-type IV in a patient with a novel mutation in the KLF1 gene: a case report and review of the literature. J Pediatr Hematol Oncol 42:e536–e540. https://doi.org/10.1097/MPH.0000000000001727
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Erythroid Krüppel-Like Factor (KLF1): A Surprisingly Versatile Regulator of Erythroid Differentiation;Advances in Experimental Medicine and Biology;2024
2. Molecular and haematological characterisation of haemolytic anaemia associated with biallelic KLF1 mutations: a case series;Journal of Clinical Pathology;2023-07-28
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