COHEN, L., TZUR, S., GOLDENBERG-COHEN, N., BORMANS, C., BEHAR, D. M., & REINSTEIN, E. (2016). Exome sequencing identified a novel de novo OPA1 mutation in a consanguineous family presenting with optic atrophy. Genet Res (Camb).

COHEN, LIOR, SHAY TZUR, NITZA GOLDENBERG-COHEN, CONCETTA BORMANS, DORON M. BEHAR, and EYAL REINSTEIN. "Exome Sequencing Identified a Novel De Novo OPA1 Mutation in a Consanguineous Family Presenting With Optic Atrophy." Genet Res (Camb) 2016.

COHEN, LIOR, et al. "Exome Sequencing Identified a Novel De Novo OPA1 Mutation in a Consanguineous Family Presenting With Optic Atrophy." Genet Res (Camb) 2016.