Mutational analysis of the RPGRIP1L gene in patients with Joubert syndrome and nephronophthisis.
Wolf, M. T. F.; Saunier, S.; O'Toole, J. F.; Wanner, N.; Groshong, T.; Attanasio, M.; Salomon, R.; Stallmach, T.; Sayer, J. A.; Waldherr, R.; Griebel, M.; Oh, J.; Neuhaus, T. J.; Josefiak, U.; Antignac, C.; Otto, E. A.; Hildebrandt, F.; Kidney International, 2007, vol. 72, issue 12, p 1520, ISSN 00852538. ISBN 00852538.

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