Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11)

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 journalArticlepeer-review

93 Scopus citations

Fingerprint

Dive into the research topics of 'Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11)'. Together they form a unique fingerprint.

Medicine & Life Sciences