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. Author manuscript; available in PMC: 2014 Nov 18.
Published in final edited form as: Mov Disord. 2013 Nov 12;29(1):154–155. doi: 10.1002/mds.25713

Figure 1. Family trees for individuals with novel variants in GNAL.

Figure 1

Genetic pedigrees for individuals with novel variants in GNAL. Affected family members are marked by shaded symbols. The variant found is indicated under the pedigree with transcript ID. Mutational status is indicated by ‘m’ for heterozygous mutation carriers and ‘wt’ for homozygous wildtype alleles. Index cases included in the initial screening are marked with an asterisk.