Literature DB >> 13680176

Triplication (/alphaalphaalpha anti3.7) or deletion (-alpha3.7/) association in Argentinian beta-thalassemic carriers.

I M Bragós1, N I Noguera, M P Raviola, A C Milani.   

Abstract

Prevalence of alpha gene triplication or deletion in beta-thalassemia carriers was studied in 109 unrelated individuals in Rosario, Argentina. In different populations -alpha(3.7) allele presents a higher prevalence than alphaalphaalpha(anti3.7); thus, alpha-thalassemia associated with beta-thalassemia is more frequently observed. Nevertheless, this event was detected in only one case (0.9%), while the association with alpha triplication was present in two subjects (1.8%).

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Year:  2003        PMID: 13680176     DOI: 10.1007/s00277-003-0738-6

Source DB:  PubMed          Journal:  Ann Hematol        ISSN: 0939-5555            Impact factor:   3.673


  2 in total

1.  Alpha-globin gene triplication and its effect in beta-thalassemia carrier, sickle cell trait, and healthy individual.

Authors:  Mohammad Hamid; Bijan Keikhaei; Hamid Galehdari; Alihossein Saberi; Alireza Sedaghat; Gholamreza Shariati; Marziye Mohammadi-Anaei
Journal:  EJHaem       Date:  2021-07-19

2.  The Frequency and Importance of Common α-globin Gene Deletions Among β-Thalassemia Carriers in an Iranian Population.

Authors:  Azam Moosavi; Ali M Ardekani
Journal:  Avicenna J Med Biotechnol       Date:  2017 Oct-Dec
  2 in total

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