Changes in HbA2 and HbF in alpha thalassemia carriers with KLF1 mutation-Reference-Cited by-同舟云学术

Changes in HbA2 and HbF in alpha thalassemia carriers with KLF1 mutation

Published:2017-05 Issue: Volume:64 Page:30-32
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Satta Stefania,Paglietti Maria Elisabetta,Sollaino Maria Carla,Barella Susanna,Moi Paolo,Desogus Maria Franca,Demartis Franca Rosa,Manunza Laura,Origa Raffaella

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference25 articles.

1. Disorders of Hemoglobin;Steinberg,2009

2. Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin;Borg;Nat. Genet.,2010

3. Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrin;Satta;Haematologica,2011

4. KLF1 gene mutations cause borderline HbA(2);Perseu;Blood,2011

5. KLF1 gene mutations in Chinese adults with increased fetal hemoglobin;Wang;Hemoglobin,2013

Cited by 7 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. Identification and Functional Analysis of Known and New Mutations in the Transcription Factor KLF1 Linked with β-Thalassemia-like Phenotypes;Biology;2023-03-28

3. Problem of borderline hemoglobin A2 levels in an Iranian population with a high prevalence of α- and β-thalassemia carriers;Egyptian Journal of Medical Human Genetics;2022-03-11

4. Association Between Genetic Polymorphisms and Hb F Levels in Heterozygous β-Thalassemia 3.5 kb Deletions;Hemoglobin;2020-09-02

5. Congenital Nonspherocytic Hemolytic Anemia Caused by Krüppel-Like Factor 1 Gene Variants: Another Case Report;Hemoglobin;2019-09-03