Cite
Genome sequencing identifies a non-coding variant in the MCDR1 locus as a cause of macular dystrophy.
MLA
Ellingford, Jamie M., et al. “Genome Sequencing Identifies a Non-Coding Variant in the MCDR1 Locus as a Cause of Macular Dystrophy.” Clinical & Experimental Ophthalmology, vol. 45, no. 3, Apr. 2017, pp. 297–99. EBSCOhost, https://doi.org/10.1111/ceo.12825.
APA
Ellingford, J. M., Sergouniotis, P. I., Jenkins, E., & Black, G. C. (2017). Genome sequencing identifies a non-coding variant in the MCDR1 locus as a cause of macular dystrophy. Clinical & Experimental Ophthalmology, 45(3), 297–299. https://doi.org/10.1111/ceo.12825
Chicago
Ellingford, Jamie M, Panagiotis I Sergouniotis, Emma Jenkins, and Graeme C Black. 2017. “Genome Sequencing Identifies a Non-Coding Variant in the MCDR1 Locus as a Cause of Macular Dystrophy.” Clinical & Experimental Ophthalmology 45 (3): 297–99. doi:10.1111/ceo.12825.