Clinical Study

The MFN2 V705I Variant Is Not a Disease-Causing Mutation: A Segregation Analysis in a CMT2 Family

Figure 2

Subtractive fluorescent difference plots of affected and unaffected family members and unrelated controls for exon 18. Both healthy family members and affected individuals grouped with control individuals (grey). Patient IV-6 showed a different melt curve profile and formed a separate melt shape (red) reflecting the presence of the V705I variant.
495873.fig.002a
(a)
495873.fig.002b
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