rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients
Author:
Affiliation:
1. Université de Tunis El Manar, Institut Pasteur de Tunis, Laboratoire d'Hématologie Moléculaire et Cellulaire, Tunisia
2. Université de Tunis El Manar, Hopital Aziza Othmena, d'Hématologie Clinique, Tunisia
Publisher
Informa UK Limited
Subject
Hematology,Hematology
Link
https://www.tandfonline.com/doi/pdf/10.1080/10245332.2015.1107275
Reference18 articles.
1. Human Fetal Hemoglobin Expression Is Regulated by the Developmental Stage-Specific Repressor BCL11A
2. Reactivation of Fetal Hemoglobin in Thalassemia and Sickle Cell Disease
3. Effect of Hydroxyurea on the Frequency of Painful Crises in Sickle Cell Anemia
4. Hydroxyurea for sickle cell anemia: what have we learned and what questions still remain?
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2. Impact of Genetic Polymorphisms in Modifier Genes in Determining Fetal Hemoglobin Levels in Beta-Thalassemia;Thalassemia Reports;2023-03-16
3. Correlations between Multiple SNPs and HbF Levels in β-Thalassemia Carriers;Clinical Laboratory;2023
4. Fetal hemoglobin regulating genetic variants identified in homozygous (HbSS) and heterozygous (HbSA) subjects from South Mexico;Journal of Tropical Pediatrics;2022-08-04
5. Single Nucleotide Polymorphisms in XMN1-HBG2, HBS1L-MYB, and BCL11A and Their Relation to High Fetal Hemoglobin Levels That Alleviate Anemia;Diagnostics;2022-06-02
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