Erratum: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus (Nature Genetics (2006) 38 (1242-1244))

Patrick Tarpey; Shery Thomas; Nagini Sarvananthan; Uma Mallya; Steven Lisgo; Chris J. Talbot; Eryl O. Roberts; Musarat Awan; Mylvaganam Surendran; Rebecca J. McLean; Robert D. Reinecke; Andrea Langmann; Susanne Lindner; Martina Koch; Sunila Jain; Geoffrey Woodruff; Richard P. Gale; Chris Degg; Konstantinos Droutsas; Ioannis Asproudis; Alina A. Zubcov; Christina Pieh; Colin D. Veal; Rajiv D. MacHado; Oliver C. Backhouse; Laura Baumber; Cris S. Constantinescu; Michael C. Brodsky; David G. Hunter; Richard W. Hertle; Randy J. Read; Sarah Edkins; Sarah O'Meara; Adrian Parker; Claire Stevens; Jon Teague; Richard Wooster; P. Andrew Futreal; Richard C. Trembath; Michael R. Stratton; F. Lucy Raymond; Irene Gottlob

doi:10.1038/ng0711-720

Erratum: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus (Nature Genetics (2006) 38 (1242-1244))

Patrick Tarpey
, Shery Thomas
, Nagini Sarvananthan
, Uma Mallya
, Steven Lisgo
, Chris J. Talbot
, Eryl O. Roberts
, Musarat Awan
, Mylvaganam Surendran
, Rebecca J. McLean
, Robert D. Reinecke
, Andrea Langmann
, Susanne Lindner
, Martina Koch
, Sunila Jain
, Geoffrey Woodruff
, Richard P. Gale
, Chris Degg
, Konstantinos Droutsas
, Ioannis Asproudis

Alina A. Zubcov, Christina Pieh, Colin D. Veal, Rajiv D. MacHado, Oliver C. Backhouse, Laura Baumber, Cris S. Constantinescu, Michael C. Brodsky, David G. Hunter, Richard W. Hertle, Randy J. Read, Sarah Edkins, Sarah O'Meara, Adrian Parker, Claire Stevens, Jon Teague, Richard Wooster, P. Andrew Futreal, Richard C. Trembath, Michael R. Stratton, F. Lucy Raymond, Irene Gottlob

Genomic Medicine

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

Original language	English (US)
Pages (from-to)	720
Number of pages	1
Journal	Nature Genetics
Volume	43
Issue number	7
DOIs	https://doi.org/10.1038/ng0711-720
State	Published - Jul 2011

ASJC Scopus subject areas

Genetics

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Tarpey, P., Thomas, S., Sarvananthan, N., Mallya, U., Lisgo, S., Talbot, C. J., Roberts, E. O., Awan, M., Surendran, M., McLean, R. J., Reinecke, R. D., Langmann, A., Lindner, S., Koch, M., Jain, S., Woodruff, G., Gale, R. P., Degg, C., Droutsas, K., ... Gottlob, I. (2011). Erratum: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus (Nature Genetics (2006) 38 (1242-1244)). Nature Genetics, 43(7), 720. https://doi.org/10.1038/ng0711-720

Tarpey, P, Thomas, S, Sarvananthan, N, Mallya, U, Lisgo, S, Talbot, CJ, Roberts, EO, Awan, M, Surendran, M, McLean, RJ, Reinecke, RD, Langmann, A, Lindner, S, Koch, M, Jain, S, Woodruff, G, Gale, RP, Degg, C, Droutsas, K, Asproudis, I, Zubcov, AA, Pieh, C, Veal, CD, MacHado, RD, Backhouse, OC, Baumber, L, Constantinescu, CS, Brodsky, MC, Hunter, DG, Hertle, RW, Read, RJ, Edkins, S, O'Meara, S, Parker, A, Stevens, C, Teague, J, Wooster, R, Futreal, PA, Trembath, RC, Stratton, MR, Raymond, FL & Gottlob, I 2011, 'Erratum: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus (Nature Genetics (2006) 38 (1242-1244))', Nature Genetics, vol. 43, no. 7, pp. 720. https://doi.org/10.1038/ng0711-720

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title = "Erratum: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus (Nature Genetics (2006) 38 (1242-1244))",

author = "Patrick Tarpey and Shery Thomas and Nagini Sarvananthan and Uma Mallya and Steven Lisgo and Talbot, \{Chris J.\} and Roberts, \{Eryl O.\} and Musarat Awan and Mylvaganam Surendran and McLean, \{Rebecca J.\} and Reinecke, \{Robert D.\} and Andrea Langmann and Susanne Lindner and Martina Koch and Sunila Jain and Geoffrey Woodruff and Gale, \{Richard P.\} and Chris Degg and Konstantinos Droutsas and Ioannis Asproudis and Zubcov, \{Alina A.\} and Christina Pieh and Veal, \{Colin D.\} and MacHado, \{Rajiv D.\} and Backhouse, \{Oliver C.\} and Laura Baumber and Constantinescu, \{Cris S.\} and Brodsky, \{Michael C.\} and Hunter, \{David G.\} and Hertle, \{Richard W.\} and Read, \{Randy J.\} and Sarah Edkins and Sarah O'Meara and Adrian Parker and Claire Stevens and Jon Teague and Richard Wooster and Futreal, \{P. Andrew\} and Trembath, \{Richard C.\} and Stratton, \{Michael R.\} and Raymond, \{F. Lucy\} and Irene Gottlob",

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AU - Thomas, Shery

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AU - Mallya, Uma

AU - Lisgo, Steven

AU - Talbot, Chris J.

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AU - Awan, Musarat

AU - Surendran, Mylvaganam

AU - McLean, Rebecca J.

AU - Reinecke, Robert D.

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AU - Woodruff, Geoffrey

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AU - Degg, Chris

AU - Droutsas, Konstantinos

AU - Asproudis, Ioannis

AU - Zubcov, Alina A.

AU - Pieh, Christina

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AU - MacHado, Rajiv D.

AU - Backhouse, Oliver C.

AU - Baumber, Laura

AU - Constantinescu, Cris S.

AU - Brodsky, Michael C.

AU - Hunter, David G.

AU - Hertle, Richard W.

AU - Read, Randy J.

AU - Edkins, Sarah

AU - O'Meara, Sarah

AU - Parker, Adrian

AU - Stevens, Claire

AU - Teague, Jon

AU - Wooster, Richard

AU - Futreal, P. Andrew

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AU - Gottlob, Irene

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Erratum: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus (Nature Genetics (2006) 38 (1242-1244))

ASJC Scopus subject areas

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