Figure Pedigrees of the SCA42 families identified in this study

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Figure Pedigrees of the SCA42 families identified in this study Pedigrees of the SCA42 families identified in this study (A) Pedigree of family A. (B) Pedigree of family B. Probands are indicated by an arrow. Shaded symbols represent affected individuals. Individuals who had WES are indicated by an asterisk. Genotypes of the c.5144 position in CACNA1G are shown under each patient sequenced. G is the reference, and A is the p. R1715H mutation. Individuals who were unavailable for genotyping are represented in gray with dashed lines. Shaded gray individuals were reported as affected. SCA = spinocerebellar ataxia. Kathie Ngo et al. Neurol Genet 2018;4:e232 Copyright © 2018 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology.