Literature DB >> 7910050

A comparison of the allelic frequencies of ten DNA polymorphisms associated with factor VIII and factor IX genes in Thai and Western European populations.

A C Goodeve1, A Chuansumrit, W Sasanakul, P Isarangkura, F E Preston, I R Peake.   

Abstract

The frequency of five factor VIII gene intragenic and linked DNA polymorphisms and five factor IX gene intragenic polymorphisms was studied in Thai females. The polymorphisms in the FVIII gene were detected by restriction enzymes BclI, XbaI, BglI and at linked loci DX13 (DXS15) and St14 (DXS52) by BglII and TaqI, respectively, and in the FIX gene by MseI, DdeI, XmnI, TaqI and HhaI. With the exception of the BglI restriction fragment length polymorphism (RFLP), which is absent in Thais, factor VIII polymorphism frequencies were similar in Thais and Caucasians. Combined use of XbaI and TaqI/St14 resulted in a heterozygosity rate of greater than 90% in Thai females. For FIX, the recently described MseI RFLP in the 5' flanking region was the most informative polymorphism in Thais, 43% of females being heterozygous. The other four polymorphisms added little to the overall heterozygosity rate. The appropriate polymorphisms were used to track defective factor VIII and IX genes through 22 Thai pedigrees with haemophilia to enable carrier status to be assigned to female family members. The information obtained during this study will form the basis for carrier detection and prenatal diagnosis of haemophilia A and B by DNA polymorphism analysis in Thailand.

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Year:  1994        PMID: 7910050     DOI: 10.1097/00001721-199402000-00005

Source DB:  PubMed          Journal:  Blood Coagul Fibrinolysis        ISSN: 0957-5235            Impact factor:   1.276


  2 in total

1.  Three-Decade Successive Establishment of Care for Women/Girls from Families with Haemophilia.

Authors:  Ampaiwan Chuansumrit; Werasak Sasanakul; Nongnuch Sirachainan; Suttikarn Santiwatana; Praguywan Kadegasem; Pakawan Wongwerawattanakoon; Noppawan Tungbubpha; Juthamard Chantaraamporn
Journal:  Appl Clin Genet       Date:  2022-10-01

2.  High heterozygosity frequency of three exonic SNPs of factor V gene (F5): implications for genetic diagnosis.

Authors:  Anshul Jadli; Bipin Kulkarni; Kanjaksha Ghosh; Shrimati Shetty
Journal:  Indian J Med Res       Date:  2015-07       Impact factor: 2.375

  2 in total

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