Literature DB >> 1642317

Bantu beta s cluster haplotype predominates among Brazilian blacks.

M A Zago1, M S Figueiredo, S H Ogo.   

Abstract

We describe the combination of polymorphic restriction-enzyme sites in the beta globin gene cluster (haplotypes) for 74 chromosomes from Brazilian Blacks bearing the sickle hemoglobin gene (beta s). The three most common African beta s haplotypes account for 67 chromosomes: 49/74 (66.2%) were identified as Central African Republic (CAR or Bantu) type, 17 (23.0%) as Benin, and one as Senegal; seven chromosomes (9.5%) had minor atypical haplotypes. This distribution is different from that observed in the United States or Jamaica, where the Benin haplotype predominates, and results from different patterns of slave trades to North and South Americas. Since the beta s gene cluster polymorphisms modulate the severity of sickle cell anemia, this heterogeneity may explain differences of the clinical behavior of the disease in the United States and South America, and should also be considered in relation to other features and diseases.

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Year:  1992        PMID: 1642317     DOI: 10.1002/ajpa.1330880304

Source DB:  PubMed          Journal:  Am J Phys Anthropol        ISSN: 0002-9483            Impact factor:   2.868


  13 in total

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Authors:  Wellington Dos Santos Silva; Maria de Nazaré Klautau-Guimarães; Cesar Koppe Grisolia
Journal:  Genet Mol Biol       Date:  2010-09-01       Impact factor: 1.771

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Journal:  Genet Mol Biol       Date:  2011-07-01       Impact factor: 1.771

6.  Influence of βS-globin haplotypes and hydroxyurea on tumor necrosis factor-alpha levels in sickle cell anemia.

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7.  Haplotype of the β(S)-globin cluster in patients with sickle cell anemia at a University Hospital in the Triangulo Mineiro, Minas Gerais.

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Journal:  Rev Bras Hematol Hemoter       Date:  2015-02-02

8.  The effects of old and recent migration waves in the distribution of HBB*S globin gene haplotypes.

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Journal:  Genet Mol Biol       Date:  2016-10-03       Impact factor: 1.771

9.  Molecular analysis and association with clinical and laboratory manifestations in children with sickle cell anemia.

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10.  Comment on "Molecular analysis and association with clinical and laboratory manifestations in children with sickle cell anemia".

Authors:  Marilda Souza Goncalves
Journal:  Rev Bras Hematol Hemoter       Date:  2014-07-22
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