APA citiranje

Yusuf, I., Gliem, M., Birtel, J., Muller, P., Mangold, E., Bolz, H., & Issa, P. (2018). The retinal phenotype associated with the frequent, synonymous c.783G > A mutation in CDHR1. Association for Research in Vision and Ophthalmology.

Chicago Style (17th ed.) Citation

Yusuf, IH, M. Gliem, J. Birtel, PL Muller, E. Mangold, H. Bolz, and PC Issa. The Retinal Phenotype Associated with the Frequent, Synonymous C.783G > A Mutation in CDHR1. Association for Research in Vision and Ophthalmology, 2018.

MLA citiranje

Yusuf, IH, et al. The Retinal Phenotype Associated with the Frequent, Synonymous C.783G > A Mutation in CDHR1. Association for Research in Vision and Ophthalmology, 2018.