Fig. 1.
PCR strategy for analysis of the FXII gene. Exon-intron organization, the localization of primers, and the positions of the sequence alterations are depicted. The brackets indicate the association between the different Taq I-alleles and their associated mutations in the 5′ upstream region and exon 12, respectively. The mutations R353P,4 10586(DelG),17 and C571S3 depicted in the lower part were not detected in our group of patients.

PCR strategy for analysis of the FXII gene. Exon-intron organization, the localization of primers, and the positions of the sequence alterations are depicted. The brackets indicate the association between the different Taq I-alleles and their associated mutations in the 5′ upstream region and exon 12, respectively. The mutations R353P,4 10586(DelG),17 and C571S3 depicted in the lower part were not detected in our group of patients.

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