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PreviewIssue DateTitleAuthor(s)
2004Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardationWeaving, L.; Christodoulou, J.; Williamson, S.; Friend, K.; McKenzie, O.; Archer, H.; Evans, J.; Clarke, A.; Pelka, G.; Tam, P.; Watson, C.; Lahooti, H.; Ellaway, C.; Bennetts, B.; Leonard, H.; Gecz, J.
2001A novel missense mutation in lysosomal sulfamidase is the basis of MPS III A in a spontaneous mouse mutantBhattacharyya, R.; Gliddon, B.; Beccari, T.; Hopwood, J.; Stanley, P.
1995A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsySteinlein, O.; Mulley, J.; Propping, P.; Wallace, R.; Phillips, H.; Sutherland, G.; Scheffer, I.; Berkovic, S.
1995Molecular cloning of the cDNA encoding human skeletal muscle triadin and its localisation to chromosome 6q22-6q23Taske, N.; Eyre, H.; O'Brien, R.; Sutherland, G.; Denborough, M.; Foster, P.
1996Characterization and chromosomal localization of the human A2a adenosine receptor gene - ADORA2ALe, F.; Townsend-Nicholson, A.; Baker, E.; Sutherland, G.; Schofield, P.
1995Bovine latent transforming growth factor β1-binding protein 2: molecular cloning, identification of tissue isoforms, and immunolocalization to elastin-associated microfibrilsGibson, M.; Hatzinikolas, G.; Davis, E.; Baker, E.; Sutherland, G.; Mecham, R.
1999GPR56, a novel secretin-like human G-protein-coupled receptor geneLiu, M.; Parker, R.; Darby, K.; Eyre, H.; Copeland, N.; Crawford, J.; Gilbert, D.; Sutherland, G.; Jenkins, N.; Herzog, H.

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