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Fig. 1 | Thrombosis Journal

Fig. 1

From: A case-report of the unprovoked thrombotic event in a patient with thymoma and severe FVII deficiency

Fig. 1

Family pedigrees, genetic sequencing of F7 p.His408Gln and PROS1 p.Pro147Ala mutation. A. The family pedigree. Arrow, patients; slashed symbol, family member passed away; Circle, female; square, male. B, Chromatogram of DNA sequence covering the flank region of mutation (c.439 C > G:p.Pro147Ala) in exon 5 of PROS1 and mutation (c.1224T > G, p.His408Gln) in exon 9 of F7. The numbering of changed amino acid residue was numbered by regarding the start codon as residue 1. Het, heterozygote; Hom, homozygote; *, novel mutation

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