Figure 2. USH1C, MYO7A, and USH1G mutations identified in Israeli Arab families. For each mutation, sequence chromatograms are shown for a non-carrier individual (wt) and an affected individual homozygous for the mutant allele (mut). A: The c.497–2delA mutation of USH1C. The exon-intron boundary is marked. The deleted base is marked with an arrow on the wt trace. B: The c.700C>T (p.Q234X) mutation of MYO7A. The mutant base is marked with an arrow. C: The c.1135–1147dup mutation of MYO7A. The duplicated sequence is marked with a box. D: The c.206–207insC mutation of USH1G. The inserted base is marked with an arrow.