Identification of a novel gene, ETX1 from Xp21.1, a candidate gene for X-linked retintis pigmentosa (RP3). by Dry, K, Aldred, M, Edgar, A, Brown, J, Manson, F, Ho, M, Prosser, J, Hardwick, L, Lennon, A, Thomson, K

ADVIRC is caused by distinct mutations in BEST1 that alter pre-mRNA splicing. by Burgess, R, Maclaren, R, Davidson, A, Urquhart, J, Holder, G, Robson, A, Moore, A, Keefe, R, Black, G, Manson, F

Isolation of a retinal-expressed gene and linkage disequilibrium mapping in the RP3 type X-linked Retinitis pigmentosa region by Wright, A, Dry, K, Edgar, A, Manson, F, Aldred, M, Brown, J, Ho, M, Lennon, A, Hardwick, L, Monaco, A, Jay, M, Bird, A

Missense mutations in a retinal pigment epithelium protein, bestrophin-1, cause retinitis pigmentosa. by Davidson, A, Millar, I, Urquhart, J, Burgess-Mullan, R, Shweikh, Y, Parry, N, O'Sullivan, J, Maher, G, McKibbin, M, Downes, S, Lotery, A, Jacobson, S, Brown, P, Black, G, Manson, F