Fig. 2From: Hypermanganesemia due to mutations in SLC39A14: further insights into Mn deposition in the central nervous systemThe figure shows segregation of the novel variant by Sanger sequencing in the index case and family members. Footnote: The proband is marked with an arrow. The consanguinity is represented by a double line. Filled and unfilled symbols indicate affected and unaffected individuals, respectively. The parents are represented as a carrier statusBack to article page