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

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dc.contributor.authorTarpey, P.en
dc.contributor.authorThomas, S.en
dc.contributor.authorSarvananthan, N.en
dc.contributor.authorMallya, U.en
dc.contributor.authorLisgo, S.en
dc.contributor.authorTalbot, C. J.en
dc.contributor.authorRoberts, E. O.en
dc.contributor.authorAwan, M.en
dc.contributor.authorSurendran, M.en
dc.contributor.authorMcLean, R. J.en
dc.contributor.authorReinecke, R. D.en
dc.contributor.authorLangmann, A.en
dc.contributor.authorLindner, S.en
dc.contributor.authorKoch, M.en
dc.contributor.authorJain, S.en
dc.contributor.authorWoodruff, G.en
dc.contributor.authorGale, R. P.en
dc.contributor.authorDegg, C.en
dc.contributor.authorDroutsas, K.en
dc.contributor.authorAsproudis, I.en
dc.contributor.authorZubcov, A. A.en
dc.contributor.authorPieh, C.en
dc.contributor.authorVeal, C. D.en
dc.contributor.authorMachado, R. D.en
dc.contributor.authorBackhouse, O. C.en
dc.contributor.authorBaumber, L.en
dc.contributor.authorConstantinescu, C. S.en
dc.contributor.authorBrodsky, M. C.en
dc.contributor.authorHunter, D. G.en
dc.contributor.authorHertle, R. W.en
dc.contributor.authorRead, R. J.en
dc.contributor.authorEdkins, S.en
dc.contributor.authorO'Meara, S.en
dc.contributor.authorParker, A.en
dc.contributor.authorStevens, C.en
dc.contributor.authorTeague, J.en
dc.contributor.authorWooster, R.en
dc.contributor.authorFutreal, P. A.en
dc.contributor.authorTrembath, R. C.en
dc.contributor.authorStratton, M. R.en
dc.contributor.authorRaymond, F. L.en
dc.contributor.authorGottlob, I.en
dc.contributor.authorBastawrous, A.en
dc.date.accessioned2015-11-24T19:02:51Z
dc.date.available2015-11-24T19:02:51Z
dc.identifier.issn1061-4036-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/19842
dc.rightsDefault Licence-
dc.titleMutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus (vol 38, pg 1242, 2006)en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDoi 10.1038/Ng0711-720-
heal.identifier.secondary<Go to ISI>://000292184600021-
heal.journalNameNat Geneten
heal.journalTypepeer-reviewed-
heal.languageen-
heal.publicationDate2011-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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