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Journal of Cellular and Molecular Medicine|December 2, 2017
Identification of a novel RPGRIP1 mutation in an Iranian family with leber congenital amaurosis by exome sequencingSaber Imani, Jingliang Cheng, Abdolkarim Mobasher-Jannat, et al.Oncotarget|February 9, 2018
Genetic identification and molecular modeling characterization reveal a novel <i>PROM1</i> mutation in Stargardt4-like macular dystrophySaber Imani, Jingliang Cheng, Marzieh Dehghan Shasaltaneh, et al.Pageof 8