A mutation in DOP1B identified as a probable cause for autosomal recessive Peters anomaly in a consanguineous family. - Darbari E; Zare-Abdollahi D; Alavi A; Rezaei Kanavi M; Feizi S; Hosseini SB; Baradaran-Rafii A; Ahmadieh H; Issazadeh-Navikas S; Elahi E (Molecular vision, 2020)