Figure 3From: A novel MIPgene mutation associated with autosomal dominant congenital cataracts in a Chinese family DNA sequence chromatograms of the proband (III:15) shows a heterozygous C > T nucleotide change in exon 1 of MIP (black zrrow) which altered the Arg to a stop codon (TGA) and an unaffected individual (III:12) shows CGA at the same codon 113. Back to article page