APA (7th ed.) Citation

N, L., A, G., I, R., R, S., SC, E., S, M., . . . A, S. (2019). Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly. Nature communications, 10(1), 1180. https://doi.org/10.1038/s41467-019-08547-w

Chicago Style (17th ed.) Citation

N, Lahrouchi, et al. "Homozygous Frameshift Mutations in FAT1 Cause a Syndrome Characterized by Colobomatous-microphthalmia, Ptosis, Nephropathy and Syndactyly." Nature Communications 10, no. 1 (2019): 1180. https://doi.org/10.1038/s41467-019-08547-w.

MLA (9th ed.) Citation

N, Lahrouchi, et al. "Homozygous Frameshift Mutations in FAT1 Cause a Syndrome Characterized by Colobomatous-microphthalmia, Ptosis, Nephropathy and Syndactyly." Nature Communications, vol. 10, no. 1, 2019, p. 1180, https://doi.org/10.1038/s41467-019-08547-w.