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Journal List > Am J Hum Genet > v.32(3); May 1980

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Am J Hum Genet. 1980 May; 32(3): 348–353.
PMCID: PMC1686083
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Genetic polymorphism of the B subunit of human coagulation factor XIII.
P G Board
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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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Selected References
These references are in PubMed. This may not be the complete list of references from this article.
  • Losowsky MS, Miloszewski KJ. Factor XIII. Br J Haematol. 1977 Sep;37(1):1–5. [PubMed]
  • Schwartz ML, Pizzo SV, Hill RL, McKee PA. Human Factor XIII from plasma and platelets. Molecular weights, subunit structures, proteolytic activation, and cross-linking of fibrinogen and fibrin. J Biol Chem. 1973 Feb 25;248(4):1395–1407. [PubMed]
  • Board PG. Genetic polymorphism of the A subunit of human coagulation factor XIII. Am J Hum Genet. 1979 Mar;31(2):116–124. [PubMed]
  • Hampton JW, Cunningham GR, Bird RM. The pattern of inheritance of defective fibrinase (Factor 13). J Lab Clin Med. 1966 Jun;67(6):914–921. [PubMed]
  • Ratnoff OD, Steinberg AG. Inheritance of fibrin-stabilising-factor deficiency. Lancet. 1968 Jan 6;1(7532):25–26. [PubMed]
  • McDonagh J, McDonagh RP, Jr, Duckert F. Genetic aspects of factor XIII deficiency. Ann Hum Genet. 1971 Oct;35(2):197–206. [PubMed]
  • Lorand L, Urayama T, Atencio AC, Hsia DY. Inheritance of deficiency of fibrin-stabilizing factor (factor 13). Am J Hum Genet. 1970 Jan;22(1):89–95. [PubMed]
  • Barbui T, Rodeghiero F, Dini E, Mariani G, Paa ML, De Biasi R, Murillo RC, Umana CM. Subunits A and S inheritance in four families with congenital factor XIII deficiency. Br J Haematol. 1978 Feb;38(2):267–271. [PubMed]
  • Israels ED, Paraskevas F, Israels LG. Immunological studies of coagulation factor XIII. J Clin Invest. 1973 Oct;52(10):2398–2403. [PubMed]
  • Barbui T, Cartei G, Chisesi T, Dini E. Electroimmunoassay of plasma subunits-a and -s in a case of congenital fibrin stabilizing factor deficiency. Thromb Diath Haemorrh. 1974 Sep 30;32(1):124–131. [PubMed]
  • Girolami A, Burul A, Fabris F, Cappellato G, Betterle C. Studies on factor XIII antigen in congenital factor XIII deficiency. A tentative classification of the disease in two groups. Folia Haematol Int Mag Klin Morphol Blutforsch. 1978;105(1):131–141. [PubMed]
  • Lorand L, Gray AJ, Brown K, Credo RB, Curtis CG, Domanik RA, Stenberg P. Dissociation of the subunit structure of fibrin stabilizing factor during activation of the zymogen. Biochem Biophys Res Commun. 1974 Feb 27;56(4):914–922. [PubMed]
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