Cita APA (7th ed.)

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.

Cita Chicago (17th ed.)

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

Cita MLA (9th ed.)

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.