Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus Year published: 2006 | Research Type: Article Publication Author(s): Tarpey, Thomas, Sarvananthan, Mallya, Lisgo, Talbot, Roberts, Awan, Surendran, McLean, Reinecke, Langmann, Lindner, Koch, Jain, Woodruff, Gale, Bastawrous, Degg, Droutsas, Asproudis, Zubcov, Pieh, Veal, Machado, Backhouse, Baumber, Constantinescu, Brodsky, Hunter, Hertle, Read, Edkins, O'Meara, Parker, Stevens, Teague, Wooster, Futreal, Trembath, Stratton, Raymond, Gottlob, View on PubMed