Case Report

Keratitis-Ichthyosis-Deafness Syndrome, Atypical Connexin GJB2 Gene Mutation, and Peripheral T-Cell Lymphoma: More Than a Random Association?

Figure 1

A search for mutations within the connexin 26 gene GJB2 showed the heterozygous c.101T→C mutation (in red in the figure) causing the substitution of a methionine residue for threonine at position 34 (p.Met34Thr).