Khan, S. A., & Nestel, A. R. (2019). CRB1 Gene Mutation Causing Different Phenotypes of Leber Congenital Amaurosis in Siblings. J Ophthalmic Vis Res.
Citação norma ChicagoKhan, Shaheryar Ahmed, and Achim Richard Nestel. "CRB1 Gene Mutation Causing Different Phenotypes of Leber Congenital Amaurosis in Siblings." J Ophthalmic Vis Res 2019.
Citação norma MLAKhan, Shaheryar Ahmed, and Achim Richard Nestel. "CRB1 Gene Mutation Causing Different Phenotypes of Leber Congenital Amaurosis in Siblings." J Ophthalmic Vis Res 2019.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.