Literature DB >> 2714240

Genetic studies of low-abundance human plasma proteins. X. Coagulation factor XIIIB variants in blacks.

M I Kamboh1, R E Ferrell.   

Abstract

Human coagulation factor XIIIV (F XIIIB) demonstrates genetically determined-structural variation with three common and several rare alleles. Population genetics studies reveal enormous intra and interracial group variation. In the present study, using isoelectric focusing and immunoblotting, we have determined for the first time the polymorphic occurrence of F XIIIB allelic forms in a native African population, namely Nigerian Blacks. In addition, F XIIIB data have been extended to various US Black populations. The characteristic feature of the black gene pool is the relative high frequency of the F XIIIB*2 allele, the highest being in Nigerians (0.723). The F XIIIB*6 allele is present at a polymorphic level in both the US and Nigerian Blacks and appears to be a unique black allele marker. The present technique has demonstrated several new alleles designated: F XIIIB*18, FXIIIB*22, F XIIIB*23 and F XIIIB*24. Among these new alleles the F XIIIB*23 exists at polymorphic level in both the US and Nigerian Blacks and is another unique Black allele marker of potential significance in population genetics studies.

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Year:  1989        PMID: 2714240     DOI: 10.1002/elps.1150100113

Source DB:  PubMed          Journal:  Electrophoresis        ISSN: 0173-0835            Impact factor:   3.535


  1 in total

1.  Polymorphism of coagulation factor XIII B subunit: further occurrence of FXIIIB*15 in Japanese and phenotyping in bloodstains.

Authors:  N Komatsu; A Kido; Y Kimura; M Oya; Y Dobashi; K Hashimoto
Journal:  Int J Legal Med       Date:  1992       Impact factor: 2.686

  1 in total

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