Prevalence of βS-globin gene haplotypes, α-thalassemia (3.7 kb deletion) and redox status in patients with sickle cell anemia in the state of Paraná, Brazil
Author:
Affiliation:
1. Universidade Estadual Paulista, Brasil; Universidade Estadual de Maringá, Brasil
2. Universidade Estadual Paulista, Brasil
3. Universidade Estadual de Maringá, Brasil
4. Hemocentro, Brasil
Publisher
FapUNIFESP (SciELO)
Subject
Genetics,Molecular Biology
Link
http://www.scielo.br/pdf/gmb/v38n3/1415-4757-gmb-38-20140231.pdf
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4. Instruction Manual-VARIANT-HPLC β-thalassemia short program.,2006
5. Factors associated with oxidative stress in human populations;Block G;Am J Epidemiol,2002
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1. Genetic Variation and Sickle Cell Disease Severity;JAMA Network Open;2023-10-18
2. Molecular Analysis of Xmn1-Polymorphic Site ´5 to Gγ of the β-Globin Gene Cluster in a Saudi Population of Jazan Region in Correlation with Hb F Expression;Evidence-Based Complementary and Alternative Medicine;2022-03-21
3. Alpha thalassemia, but not βS-globin haplotypes, influence sickle cell anemia clinical outcome in a large, single-center Brazilian cohort;Annals of Hematology;2021-02-13
4. Sickle cell anemia in the state of Maranhão: a haplotype study;Annals of Hematology;2020-05-04
5. Association between Oxidative Stress, Genetic Factors, and Clinical Severity in Children with Sickle Cell Anemia;The Journal of Pediatrics;2018-04
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