APA (7th ed.) Citation

N, C., G, G., C, O., N, K., C, G., J, T., . . . V, L. (2016). Uncommon nucleotide excision repair phenotypes revealed by targeted high-throughput sequencing. Orphanet journal of rare diseases, 11, 26. https://doi.org/10.1186/s13023-016-0408-0

Chicago Style (17th ed.) Citation

N, Calmels, et al. "Uncommon Nucleotide Excision Repair Phenotypes Revealed by Targeted High-throughput Sequencing." Orphanet Journal of Rare Diseases 11 (2016): 26. https://doi.org/10.1186/s13023-016-0408-0.

MLA (9th ed.) Citation

N, Calmels, et al. "Uncommon Nucleotide Excision Repair Phenotypes Revealed by Targeted High-throughput Sequencing." Orphanet Journal of Rare Diseases, vol. 11, 2016, p. 26, https://doi.org/10.1186/s13023-016-0408-0.