Literature DB >> 2875755

The spectrum of beta-thalassemia genes in China and Southeast Asia.

H H Kazazian, C E Dowling, P G Waber, S Huang, W H Lo.   

Abstract

To make possible prenatal diagnosis of beta-thalassemia in China and Southeast Asia by direct detection of mutant beta-globin genes, we have determined the spectrum of mutations producing the disorder in this region of the world. Seventy-eight beta-thalassemia genes from Chinese and Southeast Asians were randomly obtained, and the relevant mutation was characterized in 76 (98%) of them. Seven different point mutations were found among the 78 genes studied. Of these seven beta-thalassemia alleles, two constitute 62%, and two others account for 29% of the total. Since only four alleles make up 91% of the mutant genes, prenatal diagnosis of beta-thalassemia in China and Southeast Asia should be feasible by simplified techniques for direct detection of point mutations.

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Year:  1986        PMID: 2875755

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  22 in total

1.  Analysis of beta-globin gene haplotypes in Asian Indians: origin and spread of beta-thalassaemia on the Indian subcontinent.

Authors:  N Y Varawalla; A C Fitches; J M Old
Journal:  Hum Genet       Date:  1992-12       Impact factor: 4.132

2.  The spectrum of beta-thalassemia mutations in Taiwan: identification of a novel frameshift mutation.

Authors:  L I Lin; K S Lin; K H Lin; H C Chang
Journal:  Am J Hum Genet       Date:  1991-04       Impact factor: 11.025

3.  The molecular basis of thalassemias.

Authors:  S Fucharoen; P Winichagoon
Journal:  Indian J Pediatr       Date:  1989 Nov-Dec       Impact factor: 1.967

4.  Marfan syndrome: defective synthesis, secretion, and extracellular matrix formation of fibrillin by cultured dermal fibroblasts.

Authors:  D M Milewicz; R E Pyeritz; E S Crawford; P H Byers
Journal:  J Clin Invest       Date:  1992-01       Impact factor: 14.808

5.  The molecular basis of beta-thalassemia in Thailand: application to prenatal diagnosis.

Authors:  S L Thein; P Winichagoon; C Hesketh; S Best; S Fucharoen; P Wasi; D J Weatherall
Journal:  Am J Hum Genet       Date:  1990-09       Impact factor: 11.025

6.  A common Chinese beta-thalassemia mutation found in a Japanese family.

Authors:  Y Naritomi; H Nakashima; M Kagimoto; Y Naito; E Yokota; T Imamura
Journal:  Hum Genet       Date:  1990-04       Impact factor: 4.132

7.  Molecular basis of beta thalassemia in south China. Strategy for DNA analysis.

Authors:  J Z Zhang; S P Cai; X He; H X Lin; H J Lin; Z G Huang; F F Chehab; Y W Kan
Journal:  Hum Genet       Date:  1988-01       Impact factor: 4.132

8.  Detection of beta-thalassemia mutations in the Chinese using amplified DNA from dried blood specimens.

Authors:  S Z Huang; X D Zhou; H Zhu; Z R Ren; Y T Zeng
Journal:  Hum Genet       Date:  1990-01       Impact factor: 4.132

9.  Frameshift mutation near the 3' end of the COL1A1 gene of type I collagen predicts an elongated Pro alpha 1(I) chain and results in osteogenesis imperfecta type I.

Authors:  M C Willing; D H Cohn; P H Byers
Journal:  J Clin Invest       Date:  1990-01       Impact factor: 14.808

Review 10.  Diagnosis of genetic disease using recombinant DNA. Supplement.

Authors:  D N Cooper; J Schmidtke
Journal:  Hum Genet       Date:  1987-09       Impact factor: 4.132

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