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 AsproudisAlina 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

Research output: Contribution to journalComment/debate

Original languageEnglish (US)
Number of pages1
JournalNature Genetics
Volume43
Issue number7
DOIs
StatePublished - Jul 1 2011

ASJC Scopus subject areas

  • Genetics

Cite this

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). https://doi.org/10.1038/ng0711-720