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Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus.

By P. Tarpey, S. Thomas, N. Sarvananthan, U. Mallya, S. Lisgo, C. J. Talbot, E. O. Roberts, M. Awan, M. Surendran, Rebecca J. McLean, R. D. Reinecke, A. Langmann, S. Lindner, M. Koch, S. Jain, G. Woodruff, R. P. Gale, C. Degg, K. Droutsas, I. Asproudis, A. A. Zubcov, C. Pieh, C.D. Veal, R. D. Machado, O. C. Backhouse, L. Baumber, C. S. Constantinescu, M. C. Brodsky, D. G. Hunter, Hertle R. W., R. J. Read, S. Edkins, S. O'Meara, A. Parker, C. Stevens, J. Teague, R. Wooster, P. A. Futreal, R. C. Trembath, M. R. Stratton, F. L. Raymond and I. Gottlob
Year: 2006
DOI identifier: 10.1038/ng1893
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