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Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11)
- Correspondence to Professor F Hildebrandt, University of Michigan Health System, 8220C MSRB III, 1150 West Medical Center Drive, Ann Arbor, MI 48109-5646, USA; fhilde{at}umich.edu
Citation
Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11)
Publication history
- Received January 26, 2009
- Revised March 18, 2009
- Accepted March 23, 2009
- First published June 8, 2009.
Online issue publication
April 27, 2016
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