Rhodopsin mutations in a Scottish retinitis pigmentosa population, including a novel splice site mutation in intron four.

Author:

Bell C,Converse C A,Hammer H M,Osborne A,Haites N E

Publisher

BMJ

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology

Reference35 articles.

1. Prevalence of retinitis pigmentosa in Maine;Bunker, C.H.; Berson, E.L.; Bromley, W.C.; Hayes, R.P.; Roderick, T.H.;AmJ Ophthalmol,1984

2. Localisation of an ADRP gene to the long arm of chromosome 3;McWilliam, P.; Farrar, G.J.; Kenna, P.; Bradley, D.G.; Humphries, M.M.; Sharp, E.M.,1989

3. A point mutation of the rhodopsin gene in one form ofretinitis pigmentosa;Dryja, T.P.; McGee, T.L.; Reichel, E.; Hahn, L.B.; Cowley, G.S.; Yandell, D.W.;Nature,1990

4. Autosomal dominant retinitis pigmentosa: molecular, genetic and clinical aspects;Humphries, P.; Farrar, G.J.; Kenna, P.;ProgRetRes,1993

5. A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa;Rosenfield, P.J.; Cowley, G.S.; McGee, T.L.; Sandberg, M.A.; Berson, E.L.; Dryja, T.P.;Nature Genet,1992

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