Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus
dc.contributor.author | Tarpey, P | en_US |
dc.contributor.author | Thomas, S | en_US |
dc.contributor.author | Sarvananthan, N | en_US |
dc.contributor.author | Mallya, U | en_US |
dc.contributor.author | Lisgo, S | en_US |
dc.contributor.author | Talbot, CJ | en_US |
dc.contributor.author | Roberts, EO | en_US |
dc.contributor.author | Awan, M | en_US |
dc.contributor.author | Surendran, M | en_US |
dc.contributor.author | McLean, RJ | en_US |
dc.contributor.author | Reinecke, RD | en_US |
dc.contributor.author | Langmann, A | en_US |
dc.contributor.author | Lindner, S | en_US |
dc.contributor.author | Koch, M | en_US |
dc.contributor.author | Jain, S | en_US |
dc.contributor.author | Woodruff, G | en_US |
dc.contributor.author | Gale, RP | en_US |
dc.contributor.author | Degg, C | en_US |
dc.contributor.author | Droutsas, K | en_US |
dc.contributor.author | Asproudis, I | en_US |
dc.contributor.author | Zubcov, AA | en_US |
dc.contributor.author | Pieh, C | en_US |
dc.contributor.author | Veal, CD | en_US |
dc.contributor.author | Machado, RD | en_US |
dc.contributor.author | Backhouse, OC | en_US |
dc.contributor.author | Baumber, L | en_US |
dc.contributor.author | Constantinescu, CS | en_US |
dc.contributor.author | Brodsky, MC | en_US |
dc.contributor.author | Hunter, DG | en_US |
dc.contributor.author | Hertle, RW | en_US |
dc.contributor.author | Read, RJ | en_US |
dc.contributor.author | Edkins, S | en_US |
dc.contributor.author | O'Meara, S | en_US |
dc.contributor.author | Parker, A | en_US |
dc.contributor.author | Stevens, C | en_US |
dc.contributor.author | Teague, J | en_US |
dc.contributor.author | Wooster, R | en_US |
dc.contributor.author | Futreal, PA | en_US |
dc.contributor.author | Trembath, RC | en_US |
dc.contributor.author | Stratton, MR | en_US |
dc.contributor.author | Raymond, FL | en_US |
dc.contributor.author | Gottlob, I | en_US |
dc.date.accessioned | 2015-05-20T12:22:19Z | |
dc.date.available | 2006-09-01 | en_US |
dc.date.issued | 2006-11 | en_US |
dc.identifier.issn | 1061-4036 | en_US |
dc.identifier.uri | http://qmro.qmul.ac.uk/xmlui/handle/123456789/7467 | |
dc.format.extent | 1242 - 1244 | en_US |
dc.relation.ispartof | NAT GENET | en_US |
dc.subject | MOTOR NYSTAGMUS | en_US |
dc.subject | MODEL | en_US |
dc.subject | GENE | en_US |
dc.title | Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus | en_US |
dc.type | Article | |
dc.identifier.doi | 10.1038/ng1893 | en_US |
pubs.issue | 11 | en_US |
pubs.notes | Not known | en_US |
pubs.volume | 38 | en_US |