Citations for
1FGS6, LJFS2, MRX27, UPF3B
Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation.
Tarpey PS, Lucy Raymond F, Nguyen LS, Rodriguez J, Hackett A, Vandeleur L, Smith R, Shoubridge C, Edkins S, Stevens C, O'meara S, Tofts C, Barthorpe S, Buck G, Cole J, Halliday K, Hills K, Jones D, Mironenko T, Perry J, Varian J, West S, Widaa S, Teague J, Dicks E, Butler A, Menzies A, Richardson D, Jenkinson A, Shepherd R, Raine K, Moon J, Luo Y, Parnau J, Bhat SS, Gardner A, Corbett M, Brooks D, Thomas P, Parkinson-Lawrence E, Porteous ME, Warner JP, Sanderson T, Pearson P, Simensen RJ, Skinner C, Hoganson G, Superneau D, Wooster R, Bobrow M, Turner G, Stevenson RE, Schwartz CE, Andrew Futreal P, Srivastava AK, Stratton MR, Gecz J.
Nat Genet 39(9):1127-33. Epub 2007 Aug 19. 2007
2MRX27
Genetic localisation of MRX27 to Xq24-26 defines another discrete gene for non-specific X-linked mental retardation.
Gedeon AK, Glass IA, Connor JM, Mulley JC.
Am J Med Genet 64(1):121-4. 1996
3MRX27
Invited editorial : X-linked mental retardation : in pursuit of a gene map.
Schwartz CE.
Am J Hum Genet 52 : 1025-1031. 1993
4MRX27
XLMR genes : update 1990.
Neri G, et al.
Am J Med Genet 38 : 186-189. 1991
5MRX27
Linkage analysis in a large family with nonspecific X-linked mental retardation.
Glass LA, et al.
Am J Med Genet 38 : 240-243. 1991
6MRX27
X linked mental retardation.
Glass IA.
J Med Genet 28 : 361-371. 1991
7MRX27
Non-specific X linked mental retardation.
Kerr B, et al.
J Med Genet 28 : 378-382. 1991