Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus (vol 38, pg 1242, 2006) (Journal article)

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.

Institution and School/Department of submitter: Πανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικής
ISSN: 1061-4036
Link: <Go to ISI>://000292184600021
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά)

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