Clinical Study

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

Figure 1

Pedigree of family CMT105. Circles and squares denote females and males, respectively. Open symbols indicate unaffected individuals and solid symbols indicate affected individuals. Symbols with diagonal lines denote deceased individuals. Symbols with question mark denote unknown phenotype. Asterisks denote family members recruited for the study. The V705I variant was initially detected in the index patient IV-6 (arrow).
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