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Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11)
  1. 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
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Citation

Otto EA, Tory K, Attanasio M, et al
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 
October 01, 2009

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