APA (7th ed.) Citation

Escher, P., Passarin, O., Munier, F. L., Tran, V. H., & Vaclavik, V. (2018). Variability in clinical phenotypes of PRPF8 -linked autosomal dominant retinitis pigmentosa correlates with differential PRPF8/SNRNP200 interactions. Ophthalmic Genetics, 39(1), 80. https://doi.org/10.1080/13816810.2017.1393825

Chicago Style (17th ed.) Citation

Escher, Pascal, Olga Passarin, Francis L. Munier, Viet H. Tran, and Veronika Vaclavik. "Variability in Clinical Phenotypes of PRPF8 -linked Autosomal Dominant Retinitis Pigmentosa Correlates with Differential PRPF8/SNRNP200 Interactions." Ophthalmic Genetics 39, no. 1 (2018): 80. https://doi.org/10.1080/13816810.2017.1393825.

MLA (9th ed.) Citation

Escher, Pascal, et al. "Variability in Clinical Phenotypes of PRPF8 -linked Autosomal Dominant Retinitis Pigmentosa Correlates with Differential PRPF8/SNRNP200 Interactions." Ophthalmic Genetics, vol. 39, no. 1, 2018, p. 80, https://doi.org/10.1080/13816810.2017.1393825.