E, D., D, Z., A, A., M, R. K., S, F., SB, H., . . . E, E. (2020). A mutation in DOP1B identified as a probable cause for autosomal recessive Peters anomaly in a consanguineous family. Molecular vision, 26, 757.
Chicago Style (17th ed.) CitationE, Darbari, et al. "A Mutation in DOP1B Identified as a Probable Cause for Autosomal Recessive Peters Anomaly in a Consanguineous Family." Molecular Vision 26 (2020): 757.
MLA (9th ed.) CitationE, Darbari, et al. "A Mutation in DOP1B Identified as a Probable Cause for Autosomal Recessive Peters Anomaly in a Consanguineous Family." Molecular Vision, vol. 26, 2020, p. 757.
Warning: These citations may not always be 100% accurate.