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Dive into the research topics of 'Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11)'. Together they form a unique fingerprint.- Sort by
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E. A. Otto, K. Tory, M. Attanasio, W. Zhou, M. Chaki, Y. Paruchuri, E. L. Wise, M. T F Wolf, B. Utsch, C. Becker, G. Nürnberg, P. Nürnberg, A. Nayir, S. Saunier, C. Antignac, F. Hildebrandt
Research output: Contribution to journal › Article › peer-review