Please use this identifier to cite or link to this item:
Title: Diversity of the 5′ β-globin haplotype of four β-thalassemia mutations in the Mexican population
Author: Morales, K.R.
Magana, M.T.
Ibarra, B.
Perea, F.J.
Issue Date: 2009
Abstract: β-Globin haplotypes have been used to investigate the origin and spread of β-globin mutations such as Hb S [β6(A3)Glu→Val, GAG>GTG], Hb E [β26(B8)Glu→Lys, GAG>AAG], and β-thalassemia (β-thal). Molecular analyses revealed the presence of 17 β-thal mutations in the Mexican population; the most frequent of these are the nonsense codon 39 (C>T), IVS-I-1 (G>A), IVS-I-110 (G>A), and -28 (A>C). To improve our knowledge about their origin, we analyzed the 5′ haplotypes by restriction fragment length polymorphism. The codon 39 mutation (n = 17) was observed with five 5′ haplotypes: 1 (59%), 2 (23%), and 4, 6, and 9 (6% each). The IVS-I-1 mutation (n = 15) was found with five 5′ haplotypes: 1 (73.6%), 2, 3, 5, and 11 (6.6% each), whereas the IVS-I-110 (n = 9) and -28 mutations (n = 1) were only associated with haplotype 1. In the population studied, the codon 39 and IVS-I-1 mutations show a multicentric origin, whereas the IVS-I-110 and -28 mutations have an apparent single origin. Further investigation is required for the analysis of the polymorphisms surrounding the β-globin gene. Copyright © Informa Healthcare USA, Inc.
Appears in Collections:Producción científica UdeG (prueba)

Files in This Item:
There are no files associated with this item.

Items in RIUdeG are protected by copyright, with all rights reserved, unless otherwise indicated.