Cita APA

Khan, S. A., & Nestel, A. R. (2019). CRB1 Gene Mutation Causing Different Phenotypes of Leber Congenital Amaurosis in Siblings. J Ophthalmic Vis Res.

Chicago Style Citation

Khan, Shaheryar Ahmed, i Achim Richard Nestel. "CRB1 Gene Mutation Causing Different Phenotypes of Leber Congenital Amaurosis in Siblings." J Ophthalmic Vis Res 2019.

Cita MLA

Khan, Shaheryar Ahmed, i Achim Richard Nestel. "CRB1 Gene Mutation Causing Different Phenotypes of Leber Congenital Amaurosis in Siblings." J Ophthalmic Vis Res 2019.