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(Regional West Medical Center), Bernhard Schermer(University Medical Center Freiburg), Tomoko Obara(Massachusetts General Hospital), John F. O’Toole(University of Michigan–Ann Arbor), Karl S. Hiller(Regional West Medical Center), Adelheid M. Mueller(University of Michigan–Ann Arbor), Rainer Ruf(University of Michigan–Ann Arbor), Julia Hoefele(Regional West Medical Center), Frank Beekmann(University of Michigan–Ann Arbor), Daniel Landau(Soroka Medical Center), John W. Foreman(Duke Medical Center), Judith A. Goodship(Centre for Life), Tom Strachan(Centre for Life), Andreas Kispert(Medizinische Hochschule Hannover), Matthias T. F. Wolf(Regional West Medical Center), M. F. Gagnadoux(Université Paris Cité), Hubert Nivet(Centre Hospitalier Universitaire de Tours), Corinne Antignac(Université Paris Cité), Gerd Walz(University Medical Center Freiburg), Iain A. Drummond(Massachusetts General Hospital), Thomas Benzing(University Medical Center Freiburg), Friedhelm Hildebrandt(Regional West Medical Center)
Nature Genetics
July 18, 2003
Cited by 642Open Access
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