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Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/1700

Title: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus.
Authors: Tarpey, P.
Thomas, S.
Sarvananthan, N.
Mallya, U.
Lisgo, S.
Talbot, C.J.
Roberts, E.O.
Awan, M.
Surendran, M.
McLean, Rebecca 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.
Issue Date: 2006
Citation: Nature Genetics, 2006, 38 (11), pp.1242-1244
DOI Link: 10.1038/ng1893
ISSN: 1061-4036
Links: http://hdl.handle.net/2381/1700
Type: Article
Appears in Collections:Published Articles, Dept. of Genetics
Published Articles, Dept. of Cardiovascular Sciences

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