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

Raymond, F Lucy ; Gottlob, Irene ; Tarpey, Patrick ; Thomas, Shery ; Sarvananthan, Nagini ; Mallya, Uma ; Lisgo, Steven ; Talbot, Chris J ; Roberts, Eryl O ; Awan, Musarat ; Surendran, Mylvaganam ; McLean, Rebecca J ; Reinecke, Robert D ; Langmann, Andrea ; Lindner, Susanne ; Koch, Martina ; Jain, Sunila ; Woodruff, Geoffrey ; Gale, Richard P ; 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

Nature genetics, 2006-11, Vol.38 (11), p.1242-1244 [Periódico revisado por pares]

London: Nature Publishing Group

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