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Page 1
Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus.
Tarpey P, Thomas S, Sarvananthan N, Mallya U, Lisgo S, Talbot CJ, Roberts EO, Awan M, Surendran M, McLean RJ, Reinecke RD, Langmann A, Lindner S, Koch M, Jain S, Woodruff G, Gale RP, Bastawrous A, Degg C, Droutsas K, Asproudis I, Zubcov AA, Pieh C, Veal CD, Machado RD, Backhouse OC, Baumber L, Constantinescu CS, Brodsky MC, Hunter DG, Hertle RW, Read RJ, Edkins S, O'Meara S, Parker A, Stevens C, Teague J, Wooster R, Futreal PA, Trembath RC, Stratton MR, Raymond FL, Gottlob I. Tarpey P, et al. Among authors: roberts eo. Nat Genet. 2006 Nov;38(11):1242-4. doi: 10.1038/ng1893. Epub 2006 Oct 1. Nat Genet. 2006. PMID: 17013395 Free PMC article.
Phenotypical characteristics of idiopathic infantile nystagmus with and without mutations in FRMD7.
Thomas S, Proudlock FA, Sarvananthan N, Roberts EO, Awan M, McLean R, Surendran M, Kumar AS, Farooq SJ, Degg C, Gale RP, Reinecke RD, Woodruff G, Langmann A, Lindner S, Jain S, Tarpey P, Raymond FL, Gottlob I. Thomas S, et al. Among authors: roberts eo. Brain. 2008 May;131(Pt 5):1259-67. doi: 10.1093/brain/awn046. Epub 2008 Mar 27. Brain. 2008. PMID: 18372314
The prevalence of nystagmus: the Leicestershire nystagmus survey.
Sarvananthan N, Surendran M, Roberts EO, Jain S, Thomas S, Shah N, Proudlock FA, Thompson JR, McLean RJ, Degg C, Woodruff G, Gottlob I. Sarvananthan N, et al. Among authors: roberts eo. Invest Ophthalmol Vis Sci. 2009 Nov;50(11):5201-6. doi: 10.1167/iovs.09-3486. Epub 2009 May 20. Invest Ophthalmol Vis Sci. 2009. PMID: 19458336
STUDIES ON ANTHRAX INFECTIONS IN IMMUNIZED GUINEA PIGS.
WARD MK, MCGANN VG, HOGGE AL Jr, HUFF ML, KANODE RG Jr, ROBERTS EO. WARD MK, et al. Among authors: roberts eo. J Infect Dis. 1965 Feb;115:59-67. doi: 10.1093/infdis/115.1.59. J Infect Dis. 1965. PMID: 14258478 No abstract available.