Citace podle APA

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

Styl Chicago

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

Citace podle MLA

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

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