Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination
Edgar A. Otto(University of Michigan), Friedhelm Hildebrandt(Boston Children's Hospital), Bernhard Schermer(Cologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases), Adelheid M. Mueller(University of Michigan–Ann Arbor), John W. Foreman(Duke University), Julia Hoefele(Institute of Human Genetics), Rainer Ruf(Martin-Luther-Krankenhaus), Gerd Walz(University of Freiburg), Thomas Benzing(Beth Israel Deaconess Medical Center), Matthias T. F. Wolf(Children's Medical Center), Daniel Landau(Capital District Health Authority), Karl S. Hiller(Regional West Medical Center), Corinne Antignac(Hôpital Necker-Enfants Malades), Andreas Kispert(Medizinische Hochschule Hannover), Iain A. Drummond(Mount Desert Island Biological Laboratory), Frank Beekmann(University of Michigan–Ann Arbor), John F. O’Toole(Cleveland Clinic), Judith A. Goodship(Newcastle University), M. F. Gagnadoux(Université Paris Cité), Hubert Nivet(Centre Hospitalier Universitaire de Tours), Tom Strachan(Centre for Life), Tomoko Obara(Massachusetts General Hospital)
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