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Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus (vol 38, pg 1242, 2006)
- Authors :
- Tarpey, P.
Thomas, S.
Sarvananthan, N.
Mallya, U.
Lisgo, S.
Talbot, C. J.
Roberts, E. O.
Awan, M.
Surendran, M.
McLean, R. J.
Reinecke, R. D.
Langmann, A.
Lindner, S.
Koch, M.
Jain, S.
Woodruff, G.
Gale, R. P.
Degg, C.
Droutsas, K.
Asproudis, I.
Zubcov, A. A.
Pieh, C.
Veal, C. D.
Machado, R. D.
Backhouse, O. C.
Baumber, L.
Constantinescu, C. S.
Brodsky, M. C.
Hunter, D. G.
Hertle, R. W.
Read, R. J.
Edkins, S.
O'Meara, S.
Parker, A.
Stevens, C.
Teague, J.
Wooster, R.
Futreal, P. A.
Trembath, R. C.
Stratton, M. R.
Raymond, F. L.
Gottlob, I.
Bastawrous, A.
- Publication Year :
- 2011
-
Abstract
- Nat Genet
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.od.....10561..167a23db5a2214a4276e26b839a9cd47