Brief Article
Copyright ©2010 Baishideng.
World J Gastroenterol. Aug 14, 2010; 16(30): 3847-3852
Published online Aug 14, 2010. doi: 10.3748/wjg.v16.i30.3847
Figure 1
Figure 1 Missense germline mutation of exon 11 of hPMS2 gene in the proband of H13 hereditary nonpolyposis colorectal cancer kindreds. A: The forward sequence; B: The reverse sequence. Arrow indicates the mutation site, the single basyl substitution was transversed from C to T (C>T) at the codon 511, the codon from ACG to ATG, causing the amiod acid changes from Thr>Met, the change was identified as a new single nucleotide polymorphism.