Fig. 1From: A novel missense mutation (FGG c.1168G > T) in the gamma chain of fibrinogen causing congenital hypodysfibrinogenemia with bleeding phenotypeThe Sanger sequencing results of the healthy donor (a) and patients(b) demonstrated that the single nucleotide appeared at position 1168 in the antisense strand of FGG (FGG c.1168G > T; NCBI NM_000509.6)Back to article page