Mutational analysis of the RPGRIP1L gene in patients with Joubert syndrome and nephronophthisis
Matthias T. F. Wolf(Children's Medical Center), Friedhelm Hildebrandt(Boston Children's Hospital), John A. Sayer(Newcastle University), Martin Griebel(Coriell Institute For Medical Research), Rémi Salomon(Inserm), Edgar A. Otto(University of Michigan), Corinne Antignac(Hôpital Necker-Enfants Malades), Massimo Attanasio(Bristol-Myers Squibb (United States)), Nicola Wanner(Universität Hamburg), U. Josefiak, Thomas Stallmach(University Hospital of Zurich), John F. O’Toole(Cleveland Clinic), R. Waldherr(Praxis für Humangenetik), Ted Groshong(University of Missouri Health System), Sophie Saunier(Hôpital Necker-Enfants Malades), T. Neuhaus(University of Teacher Education Lucerne), Jangsuk Oh(Heidelberg University)
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