Figure 3From: Clinical and Molecular Characterization of Ataxia with Oculomotor Apraxia Patients In Saudi Arabia Exon 7 of MRE11 gene sequence showing the location of W210C (c.630 G > C) mutation. (A) Wild type sequence. (B) Heterozygous (C) Homozygous for the mutant allele. Arrow points to the base substitution.Back to article page