Olbrich, H., M. Fliegauf, J. Hoefele, A. Kispert, E. Otto, A. Volz, M. T. Wolf, G. Sasmaz, U. Trauer, R. Reinhardt, R. Sudbrak, C. Antignac, N. Gretz, G. Walz, B. Schermer, T. Benzing, F. Hildebrandt and H. Omran: Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis. In: Nature Genetics 34, 4, 455-459 (2003).
doi: 10.1038/ng1216
The Max Planck Society does not take any responsibility for the content of this export.