Axenfeld-Rieger  Syndrome  Associated  with  Congenital
Glaucoma  and Cytochrome P4501B1 Gene Mutations

<table>DNA sequence chromatogram of <i>CYP1B1</i> exon 3 equivalent to codon 367–370. (a) The reference sequence derived from control is shown. (b) Sequence derived from ARS patient shows heterozygous c.1103G &gt; A, which predicts a codon change from CGT &gt; CAT and heterozygous p.R368H mutation.</table>

Case Reports in Medicine

fig4

Figure 4

Figure 4: Axenfeld-Rieger  Syndrome  Associated  with  Congenital
Glaucoma  and Cytochrome P4501B1 Gene Mutations 

Case Reports in Medicine

Axenfeld-Rieger Syndrome Associated with Congenital Glaucoma and Cytochrome P4501B1 Gene Mutations

Figure 4