Cita APA

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.

Citación estilo Chicago

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.

Cita MLA

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.