APA (7th ed.) Citation

El Shamieh, S., Boulanger-Scemama, E., Lancelot, M., Antonio, A., Démontant, V., Condroyer, C., . . . Zeitz, C. (2015). Targeted Next Generation Sequencing Identifies Novel Mutations in RP1 as a Relatively Common Cause of Autosomal Recessive Rod-Cone Dystrophy. BioMed Research International, 2015, 1. https://doi.org/10.1155/2015/485624

Chicago Style (17th ed.) Citation

El Shamieh, Said, et al. "Targeted Next Generation Sequencing Identifies Novel Mutations in RP1 as a Relatively Common Cause of Autosomal Recessive Rod-Cone Dystrophy." BioMed Research International 2015 (2015): 1. https://doi.org/10.1155/2015/485624.

MLA (9th ed.) Citation

El Shamieh, Said, et al. "Targeted Next Generation Sequencing Identifies Novel Mutations in RP1 as a Relatively Common Cause of Autosomal Recessive Rod-Cone Dystrophy." BioMed Research International, vol. 2015, 2015, p. 1, https://doi.org/10.1155/2015/485624.