APA (7th ed.) Citation

Calmels, N., Greff, G., Obringer, C., Kempf, N., Gasnier, C., Tarabeux, J., . . . Mazur, A. (2016). Uncommon nucleotide excision repair phenotypes revealed by targeted high-throughput sequencing. Orphanet Journal of Rare Diseases, 11, 1. https://doi.org/10.1186/s13023-016-0408-0

Chicago Style (17th ed.) Citation

Calmels, Nadège, et al. "Uncommon Nucleotide Excision Repair Phenotypes Revealed by Targeted High-throughput Sequencing." Orphanet Journal of Rare Diseases 11 (2016): 1. https://doi.org/10.1186/s13023-016-0408-0.

MLA (9th ed.) Citation

Calmels, Nadège, et al. "Uncommon Nucleotide Excision Repair Phenotypes Revealed by Targeted High-throughput Sequencing." Orphanet Journal of Rare Diseases, vol. 11, 2016, p. 1, https://doi.org/10.1186/s13023-016-0408-0.