Identification of Novel Variants in <i>LTBP2</i> and <i>PXDN</i> Using Whole-Exome Sequencing in Developmental and Congenital Glaucoma - Fig 2

<p>(a) Sanger sequencing chromatograms for the carrier III:1 and affected individual IV:2 homozygous for the mutation (b) Family pedigree and segregation of a novel frameshift mutation (c.4031_4032insA; p.Asp1345Glyfs*6) in the <i>LTBP2</i> gene in a PCG family.