Annals of Human Genetics · 1982 · 13 citations · 13 references
Life SciencesGeneticsMolecular GeneticsHuman GeneticsMedical GeneticsStatistical GeneticsCoagulation AbnormalitiesCoagulation DisordersCoagulation Factor DeficienciesGenotype-phenotype Association AnalysisGenotype-phenotype CorrelationBlood Group PolymorphismsFactor Viiia ComplexIsoelectric FocusingPolymorphism Studies
Genetic polymorphism of coagulation factor XIIIB subunit in Japanese has been described, using a thin-layer agarose gel isoelectric focusing followed by immunofixation. Phenotypes of factor XIIIB subunit were essentially classified into three common patterns A, B and AB. It is estimated that the phenotypes are determined by two codominant alleles. A new rare variant B' has been detected in Japanese. Gene frequencies calculated from 304 individuals showed FXIII-BA = 0.735, FXIII-BB = 0.252 and FXIII-BB' = 0.013, respectively. The distribution of phenotypes fitted the Hardy-Weinberg equilibrium.
13
Human Factor XIII from Plasma and Platelets
Martin L. Schwartz, Salvatore V. Pizzo, Robert L. Hill et al. · Journal of Biological Chemistry · 1973 · 447 citations · Full text
Soo Il Chung, Marc S. Lewis, J.E. Folk · Journal of Biological Chemistry · 1974 · 188 citations · Full text
Group-Specific Component: Evidence for two Subtypes of the Gc <sup>1</sup> Gene
J. Constans, M. Viau · Science · 1977 · 158 citations
Genetic polymorphism of the A subunit of human coagulation factor XIII.
PubMed · 1979 · 111 citations
The pattern of inheritance of defective fibrinase (Factor 13).
Hampton Jw, Cunningham Gr, Bird Rm · PubMed · 1966 · 30 citations