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

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.

Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/19842

Full metadata record

DC Field	Value	Language
dc.contributor.author	Tarpey, P.	en
dc.contributor.author	Thomas, S.	en
dc.contributor.author	Sarvananthan, N.	en
dc.contributor.author	Mallya, U.	en
dc.contributor.author	Lisgo, S.	en
dc.contributor.author	Talbot, C. J.	en
dc.contributor.author	Roberts, E. O.	en
dc.contributor.author	Awan, M.	en
dc.contributor.author	Surendran, M.	en
dc.contributor.author	McLean, R. J.	en
dc.contributor.author	Reinecke, R. D.	en
dc.contributor.author	Langmann, A.	en
dc.contributor.author	Lindner, S.	en
dc.contributor.author	Koch, M.	en
dc.contributor.author	Jain, S.	en
dc.contributor.author	Woodruff, G.	en
dc.contributor.author	Gale, R. P.	en
dc.contributor.author	Degg, C.	en
dc.contributor.author	Droutsas, K.	en
dc.contributor.author	Asproudis, I.	en
dc.contributor.author	Zubcov, A. A.	en
dc.contributor.author	Pieh, C.	en
dc.contributor.author	Veal, C. D.	en
dc.contributor.author	Machado, R. D.	en
dc.contributor.author	Backhouse, O. C.	en
dc.contributor.author	Baumber, L.	en
dc.contributor.author	Constantinescu, C. S.	en
dc.contributor.author	Brodsky, M. C.	en
dc.contributor.author	Hunter, D. G.	en
dc.contributor.author	Hertle, R. W.	en
dc.contributor.author	Read, R. J.	en
dc.contributor.author	Edkins, S.	en
dc.contributor.author	O'Meara, S.	en
dc.contributor.author	Parker, A.	en
dc.contributor.author	Stevens, C.	en
dc.contributor.author	Teague, J.	en
dc.contributor.author	Wooster, R.	en
dc.contributor.author	Futreal, P. A.	en
dc.contributor.author	Trembath, R. C.	en
dc.contributor.author	Stratton, M. R.	en
dc.contributor.author	Raymond, F. L.	en
dc.contributor.author	Gottlob, I.	en
dc.contributor.author	Bastawrous, A.	en
dc.date.accessioned	2015-11-24T19:02:51Z	-
dc.date.available	2015-11-24T19:02:51Z	-
dc.identifier.issn	1061-4036	-
dc.identifier.uri	https://olympias.lib.uoi.gr/jspui/handle/123456789/19842	-
dc.rights	Default Licence	-
dc.title	Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus (vol 38, pg 1242, 2006)	en
heal.type	journalArticle	-
heal.type.en	Journal article	en
heal.type.el	Άρθρο Περιοδικού	el
heal.identifier.primary	Doi 10.1038/Ng0711-720	-
heal.identifier.secondary	<Go to ISI>://000292184600021	-
heal.language	en	-
heal.access	campus	-
heal.recordProvider	Πανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικής	el
heal.publicationDate	2011	-
heal.journalName	Nat Genet	en
heal.journalType	peer-reviewed	-
heal.fullTextAvailability	TRUE	-
Appears in Collections:	Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ

Show simple item record

Files in This Item:

File	Description	Size	Format
Asproudis-2006-mutations in FRMD7.pdf		62.03 kB	Adobe PDF	View/Open Request a copy

Show simple item record

This item is licensed under a Creative Commons License

Repository of UOI "Olympias"