Literature DB >> 10090486

Beta-thalassemia in the German population: mediterranean, Asian and novel mutations. Mutations in brief no.228. Online.

G Flatz1, K Wilke, Y V Syagailo, A Eigel, J Horst.   

Abstract

The beta-thalassemia mutations of 13 unrelated heterozygous Germans who remained unidentified in a previous study of 40 subjects were investigated at the DNA level. Two Mediterranean, one Asian and three novel mutations (CD6 -G, CDs 108 /112-12nt, CDs 130/131 + GCCT) were identified. Altogether, in 30 of the 35 subjects (86%) in which a mutation in the beta-globin gene was identified, the mutation was of Mediterranean origin. The geographical distribution suggests recent migration from the Mediterranean region as cause of the high proportion of frequent Mediterranean beta-thalassemia mutations in the German population. Our results support the notion that the majority of beta-thalassemia genes in the western and central European population are of Mediterranean origin.

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Year:  1999        PMID: 10090486     DOI: 10.1002/(sici)1098-1004(1999)13:3<258::aid-humu16>3.0.co;2-4

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.878


  2 in total

1.  Hemoglobinopathies: a longitudinal study over four decades.

Authors:  Elisabeth Kohne; Enno Kleihauer
Journal:  Dtsch Arztebl Int       Date:  2010-02-05       Impact factor: 5.594

2.  Interaction of Hb South Florida (codon 1; GTG-->ATG) and HbE, with beta-thalassemia (IVS1-1; G-->A): expression of different clinical phenotypes.

Authors:  Jin-Ai Mary Anne Tan; Kim-Lian Tan; Khairul Zaman Omar; Lee-Lee Chan; Yong-Chui Wee; Elizabeth George
Journal:  Eur J Pediatr       Date:  2008-11-26       Impact factor: 3.183

  2 in total

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