Rafiullah, R., Blum, M., Berkel, S., Paramasivam, N., & Rappold, G. (2017). A novel homozygous ARL13B variant in patients with Joubert syndrome impairs its guanine nucleotide-exchange factor activity. European journal of human genetics, 25(12), . https://doi.org/10.1038/s41431-017-0031-0
Chicago Style (17th ed.) CitationRafiullah, Rafiullah, Martin Blum, Simone Berkel, Nagarajan Paramasivam, and Gudrun Rappold. "A Novel Homozygous ARL13B Variant in Patients with Joubert Syndrome Impairs Its Guanine Nucleotide-exchange Factor Activity." European Journal of Human Genetics 25, no. 12 (2017). https://doi.org/10.1038/s41431-017-0031-0.
MLA (9th ed.) CitationRafiullah, Rafiullah, et al. "A Novel Homozygous ARL13B Variant in Patients with Joubert Syndrome Impairs Its Guanine Nucleotide-exchange Factor Activity." European Journal of Human Genetics, vol. 25, no. 12, 2017, https://doi.org/10.1038/s41431-017-0031-0.