Figure 1 of Tian, Mol Vis 2019; 25:60-69.


Figure 1. Chromatograms and pedigrees of four families with familial exudative vitreoretinopathy. A, B: In family A, the c.1188_1192del (p.F396fs) was identified in a 4-year-old boy and his affected father. C, D: In family B, we identified the c.1220delC (p.A407Vfs*24) mutation in a 3-year-old boy and his affected father. E, F: In family C, the c.905G>A (p.C302Y) mutation was identified in a 3-year-old boy and his affected father. G, H: In family D, we identified the c.1325T>A (p.V442E) mutation in a 2-year-old boy and his affected father. In the pedigrees, M sign represents a variant; WT represents a normal allele; arrows, probands; squares, males; circles, females; filled symbols, affected individuals; open symbols, unaffected individuals.