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Dive into the research topics of 'Mutational analysis of the RPGRIP1L gene in patients with Joubert syndrome and nephronophthisis'. Together they form a unique fingerprint.- Sort by
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M. T F Wolf, S. Saunier, J. F. O'Toole, N. Wanner, T. Groshong, M. Attanasio, R. Salomon, T. Stallmach, J. A. Sayer, R. Waldherr, M. Griebel, J. Oh, T. J. Neuhaus, U. Josefiak, C. Antignac, E. A. Otto, F. Hildebrandt
Research output: Contribution to journal › Article › peer-review