Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11).
Otto, A.; Tory, K.; Attanasio, M.; Zhou, W.; Chaki, M.; Paruchuri, Y.; L.^Wise, E.; T.^F.^Wolf, M.; Utsch, B.; Becker, C.; Nürnberg, G.; Nürnberg, P.; Nayir, A.; Saunier, S.; Antignac, C.; Hildebrandt, F.; Journal of Medical Genetics, 2009, vol. 46, issue 10, p 663, ISSN 00222593. ISBN 14686244.

Full Text Resources Located for this Citation

View article on EBSCOhost(Login required)
View article via CrossRef