Axenfeld-Rieger Syndrome Associated with Congenital
Glaucoma and Cytochrome P4501B1 Gene Mutations
Figure 3
DNA sequence chromatogram of CYP1B1 exon 3 equivalent to codon 354–357. (a) The reference sequence derived from control is shown. (b) Sequence derived from ARS patient shows heterozygous c.1063C T, which predicts a codon change CGA TGA and heterozygous p.R355X, a non-sense mutation.
