APA (7th ed.) Citation

Mohammadi‐asl, J., Hajjari, M., Tahmasebi Birgani, M., Riahi, K., Nasiri, H., & Kollaee, A. (2018). Exome sequencing revealed a novel deletion in the ERCC8 gene in an Iranian family with Cockayne syndrome. Annals of Human Genetics, 82(5), 304. https://doi.org/10.1111/ahg.12255

Chicago Style (17th ed.) Citation

Mohammadi‐asl, J., M. Hajjari, M. Tahmasebi Birgani, K. Riahi, H. Nasiri, and A. Kollaee. "Exome Sequencing Revealed a Novel Deletion in the ERCC8 Gene in an Iranian Family with Cockayne Syndrome." Annals of Human Genetics 82, no. 5 (2018): 304. https://doi.org/10.1111/ahg.12255.

MLA (9th ed.) Citation

Mohammadi‐asl, J., et al. "Exome Sequencing Revealed a Novel Deletion in the ERCC8 Gene in an Iranian Family with Cockayne Syndrome." Annals of Human Genetics, vol. 82, no. 5, 2018, p. 304, https://doi.org/10.1111/ahg.12255.