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Journal of Medical Genetics|August 27, 1998
Assessment of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene localised to 6q13-q15 in autosomal dominant Stargardt-like disease (ADSTGD), progressive bifocal chorioretinal atrophy (PBCRA), and North Carolina macular dystrophy (MCDR1)A Gehrig, U Felbor, R E Kelsell, et al.Proceedings of the National Academy of Sciences of the United States of America|August 4, 1999
Biochemical analysis of a dimerization domain mutation in RetGC-1 associated with dominant cone-rod dystrophyC L Tucker, S C Woodcock, R E Kelsell, et al.Human Molecular Genetics|April 1, 1997
Localisation of a gene for dominant cone-rod dystrophy (CORD6) to chromosome 17pR E Kelsell, K Evans, C Y Gregory, et al.Ophthalmology|June 1, 1996
Clinical features of progressive bifocal chorioretinal atrophy: a retinal dystrophy linked to chromosome 6qB F Godley, P A Tiffin, K Evans, et al.Brain Research|February 15, 2001
The neuroprotective agent sipatrigine (BW619C89) potently inhibits the human tandem pore-domain K(+) channels TREK-1 and TRAAKH J Meadows, C G Chapman, D M Duckworth, et al.Brain Research. Molecular Brain Research|February 13, 2001
Distribution analysis of human two pore domain potassium channels in tissues of the central nervous system and peripheryA D Medhurst, G Rennie, C G Chapman, et al.The British Journal of Ophthalmology|June 19, 2003
Genetic linkage analysis of a novel syndrome comprising North Carolina-like macular dystrophy and progressive sensorineural hearing lossP J Francis, S Johnson, B Edmunds, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|November 16, 2001
Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1S M Downes, A M Payne, R E Kelsell, et al.Human Molecular Genetics|September 1, 1995
Localization of the gene for progressive bifocal chorioretinal atrophy (PBCRA) to chromosome 6qR E Kelsell, B F Godley, K Evans, et al.The British Journal of Ophthalmology|January 30, 1999
Phenotype of a British North Carolina macular dystrophy family linked to chromosome 6qM B Reichel, R E Kelsell, J Fan, et al.Pageof 2