Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis.

MLA

Olbrich, Heike, et al. “Mutations in a Novel Gene, NPHP3, Cause Adolescent Nephronophthisis, Tapeto-Retinal Degeneration and Hepatic Fibrosis.” Nature Genetics, vol. 34, no. 4, Aug. 2003, pp. 455–59. EBSCOhost, https://doi.org/10.1038/ng1216.

APA

Olbrich, H., Fliegauf, M., Hoefele, J., Kispert, A., Otto, E., Volz, A., Wolf, M. T., Sasmaz, G., Trauer, U., Reinhardt, R., Sudbrak, R., Antignac, C., Gretz, N., Walz, G., Schermer, B., Benzing, T., Hildebrandt, F., & Omran, H. (2003). Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis. Nature Genetics, 34(4), 455–459. https://doi.org/10.1038/ng1216

Chicago

Olbrich, Heike, Manfred Fliegauf, Julia Hoefele, Andreas Kispert, Edgar Otto, Andreas Volz, Matthias T Wolf, et al. 2003. “Mutations in a Novel Gene, NPHP3, Cause Adolescent Nephronophthisis, Tapeto-Retinal Degeneration and Hepatic Fibrosis.” Nature Genetics 34 (4): 455–59. doi:10.1038/ng1216.