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J Clin Invest. 2010 April 1; 120(4): 1362.
PMCID: PMC2846045
Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy
John F. O’Toole, Yangjian Liu, Erica E. Davis, Christopher J. Westlake, Massimo Attanasio, Edgar A. Otto, Dominik Seelow, Gudrun Nurnberg, Christian Becker, Matti Nuutinen, Mikko Kärppä, Jaakko Ignatius, Johanna Uusimaa, Salla Pakanen, Elisa Jaakkola, Lambertus P. van den Heuvel, Henry Fehrenbach, Roger Wiggins, Meera Goyal, Weibin Zhou, Matthias T.F. Wolf, Eric Wise, Juliana Helou, Susan J. Allen, Carlos A. Murga-Zamalloa, Shazia Ashraf, Moumita Chaki, Saskia Heeringa, Gil Chernin, Bethan E. Hoskins, Hassan Chaib, Joseph Gleeson, Takehiro Kusakabe, Takako Suzuki, R. Elwyn Isaac, Lynne M. Quarmby, Bryan Tennant, Hisashi Fujioka, Hannu Tuominen, Ilmo Hassinen, Hellevi Lohi, Judith L. van Houten, Agnes Rotig, John A. Sayer, Boris Rolinski, Peter Freisinger, Sethu M. Madhavan, Martina Herzer, Florence Madignier, Holger Prokisch, Peter Nurnberg, Peter K. Jackson, Hemant Khanna, Nicholas Katsanis, and Friedhelm Hildebrandt
 
Original citation: J. Clin. Invest.2010;120(3):791–802. doi:10.1172/JCI40076.
Citation for this corrigendum: J. Clin. Invest.2010;120(4):1362. doi:10.1172/JCI40076C1.
During the preparation of the manuscript, Peter K. Jackson’s name was inadvertently presented incorrectly in the author list. The correct author list appears above.
The authors regret the errors.
Articles from The Journal of Clinical Investigation are provided here courtesy of
American Society for Clinical Investigation