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