Skip to main content
Article thumbnail
Location of Repository

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
OAI identifier: oai:lra.le.ac.uk:2381/1700
Journal:
Download PDF:
Sorry, we are unable to provide the full text but you may find it at the following location(s):
  • https://lra.le.ac.uk/handle/23... (external link)
  • http://hdl.handle.net/2381/170... (external link)
  • Suggested articles


    To submit an update or takedown request for this paper, please submit an Update/Correction/Removal Request.