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

Tarpey, Patrick; Thomas, Shery; Sarvananthan, Nagini; Mallya, Uma; Lisgo, Steven; Talbot, Chris J; Roberts, Eryl O; Awan, Musarat; Surendran, Mylvaganam; McLean, Rebecca J; +33 more... Reinecke, Robert D; Langmann, Andrea; Lindner, Susanne; Koch, Martina; Jain, Sunila; Woodruff, Geoffrey; Gale, Richard P; Bastawrous, Andrew; Degg, Chris; Droutsas, Konstantinos; Asproudis, Ioannis; Zubcov, Alina A; Pieh, Christina; Veal, Colin D; Machado, Rajiv D; Backhouse, Oliver C; Baumber, Laura; Constantinescu, Cris S; Brodsky, Michael C; Hunter, David G; Hertle, Richard W; Read, Randy J; Edkins, Sarah; O'Meara, Sarah; Parker, Adrian; Stevens, Claire; Teague, Jon; Wooster, Richard; Futreal, P Andrew; Trembath, Richard C; Stratton, Michael R; Raymond, F Lucy; Gottlob, Irene; (2006) Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus. Nature genetics, 38 (11). pp. 1242-1244. ISSN 1061-4036 DOI: https://doi.org/10.1038/ng1893

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