Cite
Homozygosity Mapping and Whole Exome Sequencing Reveal a Novel Homozygous COL18A1 Mutation Causing Knobloch Syndrome.
MLA
Haghighi, Alireza, et al. “Homozygosity Mapping and Whole Exome Sequencing Reveal a Novel Homozygous COL18A1 Mutation Causing Knobloch Syndrome.” PLoS ONE, vol. 9, no. 11, Nov. 2014, pp. 1–8. EBSCOhost, https://doi.org/10.1371/journal.pone.0112747.
APA
Haghighi, A., Tiwari, A., Piri, N., Nürnberg, G., Saleh-Gohari, N., Haghighi, A., Neidhardt, J., Nürnberg, P., & Berger, W. (2014). Homozygosity Mapping and Whole Exome Sequencing Reveal a Novel Homozygous COL18A1 Mutation Causing Knobloch Syndrome. PLoS ONE, 9(11), 1–8. https://doi.org/10.1371/journal.pone.0112747
Chicago
Haghighi, Alireza, Amit Tiwari, Niloofar Piri, Gudrun Nürnberg, Nasrollah Saleh-Gohari, Amirreza Haghighi, John Neidhardt, Peter Nürnberg, and Wolfgang Berger. 2014. “Homozygosity Mapping and Whole Exome Sequencing Reveal a Novel Homozygous COL18A1 Mutation Causing Knobloch Syndrome.” PLoS ONE 9 (11): 1–8. doi:10.1371/journal.pone.0112747.