Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis
Heike Olbrich(University Hospital Münster), Heymut Omran(University Hospital Münster), Bernhard Schermer(Cologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases), Manfred Fliegauf(University of Freiburg), Julia Hoefele(Institute of Human Genetics), Gerd Walz(University of Freiburg), Richard Reinhardt(Cold Spring Harbor Laboratory), Ute Trauer(Max Planck Society), Thomas Benzing(Beth Israel Deaconess Medical Center), Matthias T. F. Wolf(Children's Medical Center), Edgar A. Otto(University of Michigan), Corinne Antignac(Hôpital Necker-Enfants Malades), Andreas Kispert(Medizinische Hochschule Hannover), Friedhelm Hildebrandt(Boston Children's Hospital), Ralf Sudbrak, Norbert Gretz(Heidelberg University), Gürsel Sasmaz(University of Freiburg)
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