The MFN2 V705I Variant Is Not a Disease-Causing Mutation: A Segregation Analysis in a CMT2 Family
Figure 3
Sequence chromatograms showing the V705I variant in exon 18. An asterisk denotes the base change resulting in c.2113G > A (V705I). Panels (a), (b), and (c) are sequence chromatograms of clinically affected individuals. Panel (d) is the sequence chromatogram for the wildtype allele from a control individual. Only individual IV-6 carried the variant.
