Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11)
Otto, E A, Tory, K, Attanasio, M, Zhou, W, Chaki, M, Paruchuri, Y, Wise, E L, Wolf, M T F, Utsch, B, Becker, C, Nürnberg, G, Nürnberg, P, Nayir, A, Saunier, S, Antignac, C, Hildebrandt, F
Published in Journal of medical genetics (01.10.2009)
Published in Journal of medical genetics (01.10.2009)
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