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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.
First Published: 2006
Citation: Nature Genetics, 2006, 38 (11), pp.1242-1244
DOI Link: 10.1038/ng1893
ISSN: 1061-4036
Type: Article
Appears in Collections:Published Articles, Dept. of Cardiovascular Sciences
Published Articles, Dept. of Genetics

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