Fig. 1From: Novel pyrroline-5-carboxylate reductase 2 (PYCR2) mutation in an Iranian patient with hypomyelinating leukodystrophy: findings of molecular and in silico investigationsPedigree of the family described in this study. The studied patient (proband, V.1) is shown with the arrow. In addition, the III.1, III.2, and III.3 individuals had microcephaly phenotypesBack to article page