Fig. 1From: The homozygous pathogenic variant of the POMGNT1 gene identified using whole-exome sequencing in Iranian family with congenital hydrocephalusPedigree of the nuclear family with four affected siblings and extended family members. On the pedigree, the genotypes of the consanguineous parents and their afflicted offspring for the c.74 G>A variation are displayed. The afflicted proband is denoted by the arrow. Abbreviations: Wks: Weeks; A: Adenine; G: GuanineBack to article page