Sickle cell anemia: clinical diversity and beta S-globin haplotypes
- PMID: 23904799
- PMCID: PMC3728122
- DOI: 10.5581/1516-8484.20130048
Sickle cell anemia: clinical diversity and beta S-globin haplotypes
Conflict of interest statement
Conflict-of-interest disclosure: The authors declare no competing financial interest
Comment on
- Kidney dysfunction and beta S-haplotypes in patients with sickle cell disease. :171–173.
References
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- Srinivas R, Dunda O, Krishnamoorthy R, Fabry ME, Georges A, Labie D, et al. Atypical haplotypes linked to the beta-S gene in Africa are likely to be the product of recombination. Am J Hematol. 1988;29(1):60–62. - PubMed
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- Zago MA, Figueiredo MS, Ogo SH. Bantu beta-S cluster haplotype predominates among Brazilian blacks. Am J Phys Anthropol. 1992;88(3):295–298. - PubMed
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- Zago MA, Silva-Júnior WA, Dalle B, Gualandro S, Hutz MH, Lapoumeroulie C, et al. Atypical beta-S haplotypes are generated by diverse genetic mechanisms. Am J Hematol. 2000;63(2):79–84. - PubMed
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