Novel Mutations in MLH1 and MSH2 Genes in Mexican Patients with Lynch Syndrome

<div>DNA sequencing results in three LS patients. (a) Patient LS-23 with c.2103+1G&gt;C in the MLH1 gene. (b) Patient LS-41 with two different mutations in the MLH1 gene: c.1852_1854delAAG (p.K618del) and c.1852_1853delinsGC (p.K618A). (c) Patient LS-52 with mutation c.638dupT in the MSH2 gene. The arrows indicate the location of the mutations.</div>

Gastroenterology Research and Practice

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Figure 2

Figure 2: Novel Mutations in MLH1 and MSH2 Genes in Mexican Patients with Lynch Syndrome