Fig. 1From: Novel deep intronic mutation in the coagulation factor XIII a chain gene leading to unexpected RNA splicing in a patient with factor XIII deficiencyIdentification of F13A1 mutation. A, the family tree. B, Sanger sequences for the proband (homozygote), mother/father (heterozygote), and unaffected control. C, the results of Human Splicing Finder. Both prediction algorithms of the new acceptor site indicate the potential alteration of splicingBack to article page