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. 1980 May;32(3):348-53.

Genetic polymorphism of the B subunit of human coagulation factor XIII

Genetic polymorphism of the B subunit of human coagulation factor XIII

P G Board. Am J Hum Genet. 1980 May.

Abstract

Genetic variation of the B subunit of human coagulation factor XIII has been observed after electrophoresis of plasma or serum samples on thin layer agarose plates and subsequent immunofixation with a specific antiserum. The F-XIIIB locus is autosomal and has three alleles. In Australian blood donors, the F-XIIIB1, F-XIIIB2 and F-XIIIB3 alleles have frequencies of .747, .084, and .169, respectively.

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