Compound heterozygosity for KLF1 mutations is associated with microcytic hypochromic anemia and increased fetal hemoglobin-Reference-Cited by-同舟云学术

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Compound heterozygosity for KLF1 mutations is associated with microcytic hypochromic anemia and increased fetal hemoglobin

Published:2015-01-14 Issue:10 Volume:23 Page:1341-1348
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Huang Jiwei,Zhang Xinhua,Liu Dun,Wei Xiaofeng,Shang Xuan,Xiong Fu,Yu Lihua,Yin Xiaolin,Xu Xiangmin

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/ejhg2014291.pdf

Reference25 articles.

1. Alaarg A, Schiffelers RM, van Solinge WW, van Wijk R : Red blood cell vesiculation in hereditary hemolytic anemia. Front Physiol 2013; 4: 365.

2. Higgs DR, Engel JD, Stamatoyannopoulos G : Thalassaemia. Lancet 2012; 379: 373–383.

3. Cappellini MD, Fiorelli G : Glucose-6-phosphate dehydrogenase deficiency. Lancet 2008; 371: 64–74.

4. Jung HL : A new paradigm in the diagnosis of hereditary hemolytic anemia. Blood Res 2013; 48: 237–239.

5. Iolascon A, Russo R, Delaunay J : Congenital dyserythropoietic anemias. Curr Opin Hematol 2011; 18: 146–151.

Cited by 29 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. Mutations in linker-2 of KLF1 impair expression of membrane transporters and cytoskeletal proteins causing hemolysis;Nature Communications;2024-08-15

2. Molecular and haematological characterisation of haemolytic anaemia associated with biallelic KLF1 mutations: a case series;Journal of Clinical Pathology;2023-07-28

3. Identification of a genomic DNA sequence that quantitatively modulates KLF1 transcription factor expression in differentiating human hematopoietic cells;Scientific Reports;2023-05-10

4. Hematopoietic cell transplantation for congenital dyserythropoietic anemia IV caused by compound heterozygous KLF1 mutations;Annals of Hematology;2023-03-31

5. Whole exome sequencing and rare variant association study to identify genetic modifiers, KLF1 mutations, and a novel double mutation in Thai patients with hemoglobin E/beta-thalassemia;Hematology;2023-03-20

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