Fig. 1From: Spinocerebellar ataxia type 14 (SCA14) in an Argentinian family: a case reportPedigree. Index patient is individual II-2. Affected individuals are shown by shaded symbols. Deceased individuals are indicated by a line. Genotypes of the PRKCG gene are shown. G represents the reference while A is the p.Gln127Arg mutation. Affected family members and their corresponding phenotypes are indicated. *Gait ataxia, limb ataxia, horizontal nystagmus, ophthalmoplegia. ^Hyper-reflexiaBack to article page