Fig. 3From: SLC20A2-Associated Idiopathic basal ganglia calcification (Fahr disease): a case family reportMolecular genetic test report. The proband (II: 3), father (I: 1), second sister (II: 2) and younger brother II:4) share heterozygous mutations in the SLC20A2 gene (c.1097delG p.G366fs*89) and the mother (I: 2) and the elder sister(II: 1) was wild-typeBack to article page