Erratum: Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy (Journal of Clinical Investigation (2010) 120, 3 (791-802) DOI: 10.1172/JCI40076)

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; 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; Friedhelm Hildebrandt

doi:10.1172/JCI40076C1

Erratum: Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy (Journal of Clinical Investigation (2010) 120, 3 (791-802) DOI: 10.1172/JCI40076)

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, Weibin Zhou, Matthias T F WolfEric 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, Friedhelm Hildebrandt

Research output: Contribution to journal › Comment/debate › peer-review

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Original language	English (US)
Pages (from-to)	1362
Number of pages	1
Journal	Journal of Clinical Investigation
Volume	120
Issue number	4
DOIs	https://doi.org/10.1172/JCI40076C1
State	Published - Apr 1 2010

ASJC Scopus subject areas

Medicine(all)

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O'Toole, J. F., Liu, Y., Davis, E. E., Westlake, C. J., Attanasio, M., Otto, E. A., Seelow, D., Nurnberg, G., Becker, C., Nuutinen, M., Kärppä, M., Ignatius, J., Uusimaa, J., Pakanen, S., Jaakkola, E., Van Den Heuvel, L. P., Fehrenbach, H., Wiggins, R., Zhou, W., ... Hildebrandt, F. (2010). Erratum: Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy (Journal of Clinical Investigation (2010) 120, 3 (791-802) DOI: 10.1172/JCI40076). Journal of Clinical Investigation, 120(4), 1362. https://doi.org/10.1172/JCI40076C1

Erratum : Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy (Journal of Clinical Investigation (2010) 120, 3 (791-802) DOI: 10.1172/JCI40076). / O'Toole, John F.; Liu, Yangjian; Davis, Erica E. et al.

In: Journal of Clinical Investigation, Vol. 120, No. 4, 01.04.2010, p. 1362.

Research output: Contribution to journal › Comment/debate › peer-review

O'Toole, JF, Liu, Y, Davis, EE, Westlake, CJ, Attanasio, M, Otto, EA, Seelow, D, Nurnberg, G, Becker, C, Nuutinen, M, Kärppä, M, Ignatius, J, Uusimaa, J, Pakanen, S, Jaakkola, E, Van Den Heuvel, LP, Fehrenbach, H, Wiggins, R, Zhou, W, Wolf, MTF, Wise, E, Helou, J, Allen, SJ, Murga-Zamalloa, CA, Ashraf, S, Chaki, M, Heeringa, S, Chernin, G, Hoskins, BE, Chaib, H, Gleeson, J, Kusakabe, T, Suzuki, T, Isaac, RE, Quarmby, LM, Tennant, B, Fujioka, H, Tuominen, H, Hassinen, I, Lohi, H, Van Houten, JL, Rotig, A, Sayer, JA, Rolinski, B, Freisinger, P, Madhavan, SM, Herzer, M, Madignier, F, Prokisch, H, Nurnberg, P, Jackson, PK, Khanna, H, Katsanis, N & Hildebrandt, F 2010, 'Erratum: Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy (Journal of Clinical Investigation (2010) 120, 3 (791-802) DOI: 10.1172/JCI40076)', Journal of Clinical Investigation, vol. 120, no. 4, pp. 1362. https://doi.org/10.1172/JCI40076C1

O'Toole JF, Liu Y, Davis EE, Westlake CJ, Attanasio M, Otto EA et al. Erratum: Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy (Journal of Clinical Investigation (2010) 120, 3 (791-802) DOI: 10.1172/JCI40076). Journal of Clinical Investigation. 2010 Apr 1;120(4):1362. https://doi.org/10.1172/JCI40076C1

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author = "O'Toole, {John F.} and Yangjian Liu and Davis, {Erica E.} and Westlake, {Christopher J.} and Massimo Attanasio and Otto, {Edgar A.} and Dominik Seelow and Gudrun Nurnberg and Christian Becker and Matti Nuutinen and Mikko K{\"a}rpp{\"a} and Jaakko Ignatius and Johanna Uusimaa and Salla Pakanen and Elisa Jaakkola and {Van Den Heuvel}, {Lambertus P.} and Henry Fehrenbach and Roger Wiggins and Weibin Zhou and Wolf, {Matthias T F} and Eric Wise and Juliana Helou and Allen, {Susan J.} and Murga-Zamalloa, {Carlos A.} and Shazia Ashraf and Moumita Chaki and Saskia Heeringa and Gil Chernin and Hoskins, {Bethan E.} and Hassan Chaib and Joseph Gleeson and Takehiro Kusakabe and Takako Suzuki and Isaac, {R. Elwyn} and Quarmby, {Lynne M.} and Bryan Tennant and Hisashi Fujioka and Hannu Tuominen and Ilmo Hassinen and Hellevi Lohi and {Van Houten}, {Judith L.} and Agnes Rotig and Sayer, {John A.} and Boris Rolinski and Peter Freisinger and Madhavan, {Sethu M.} and Martina Herzer and Florence Madignier and Holger Prokisch and Peter Nurnberg and Jackson, {Peter K.} and Hemant Khanna and Nicholas Katsanis and Friedhelm Hildebrandt",

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AU - Liu, Yangjian

AU - Davis, Erica E.

AU - Westlake, Christopher J.

AU - Attanasio, Massimo

AU - Otto, Edgar A.

AU - Seelow, Dominik

AU - Nurnberg, Gudrun

AU - Becker, Christian

AU - Nuutinen, Matti

AU - Kärppä, Mikko

AU - Ignatius, Jaakko

AU - Uusimaa, Johanna

AU - Pakanen, Salla

AU - Jaakkola, Elisa

AU - Van Den Heuvel, Lambertus P.

AU - Fehrenbach, Henry

AU - Wiggins, Roger

AU - Zhou, Weibin

AU - Wolf, Matthias T F

AU - Wise, Eric

AU - Helou, Juliana

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AU - Chernin, Gil

AU - Hoskins, Bethan E.

AU - Chaib, Hassan

AU - Gleeson, Joseph

AU - Kusakabe, Takehiro

AU - Suzuki, Takako

AU - Isaac, R. Elwyn

AU - Quarmby, Lynne M.

AU - Tennant, Bryan

AU - Fujioka, Hisashi

AU - Tuominen, Hannu

AU - Hassinen, Ilmo

AU - Lohi, Hellevi

AU - Van Houten, Judith L.

AU - Rotig, Agnes

AU - Sayer, John A.

AU - Rolinski, Boris

AU - Freisinger, Peter

AU - Madhavan, Sethu M.

AU - Herzer, Martina

AU - Madignier, Florence

AU - Prokisch, Holger

AU - Nurnberg, Peter

AU - Jackson, Peter K.

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AU - Katsanis, Nicholas

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Erratum: Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy (Journal of Clinical Investigation (2010) 120, 3 (791-802) DOI: 10.1172/JCI40076)

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