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PreviewIssue DateTitleAuthor(s)
2007Reduced cortical inhibition in a mouse model of familial childhood absence epilepsyTan, H.; Reid, C.; Single, F.; Davies, P.; Chiu, C.; Murphy, S.; Clarke, A.; Dibbens, L.; Krestel, H.; Mulley, J.; Jones, M.; Seeburg, P.; Sakmann, B.; Berkovic, S.; Sprengel, R.; Petrou, S.
1998Febrile seizures and generalised epilepsy associated with a mutation in the Na+-channel b1 subunit gene SCN1BWallace, R.; Wang, D.; Singh, R.; Scheffer, I.; George Jnr., A.; Phillips, H.; Saar, K.; Reis, A.; Johnson, E.; Sutherland, G.; Berkovic, S.; Mulley, J.
2010A focal Eeilepsy and intellectual disability syndrome is due to a mutation in TBC1D24Bahlo, M.; Jolly, L.; Afawi, Z.; Gardner, A.; Oliver, K.; Tan, S.; Coffey, A.; Mulley, J.; Dibbens, L.; Simri, W.; Shalata, A.; Kivity, S.; Jackson, G.; Berkovic, S.; Gecz, J.; Corbett, M.
2002Truncation of the GABAA-receptor γ2 subunit in a family with generalized epilepsy with febrile seizures plusHarkin, L.; Bowser, D.; Dibbens, L.; Singh, R.; Phillips, F.; Wallace, R.; Richards, M.; Williams, D.; Mulley, J.; Berkovic, S.; Scheffer, I.; Petrou, S.
2001CHRNB2 is the second acetylcholine receptor subunit associated with autosomal dominant nocturnal frontal lobe epilepsyPhillips, H.; Favre, I.; Kirkpatrick, M.; Zuberi, S.; Goudie, D.; Heron, S.; Scheffer, I.; Sutherland, G.; Berkovic, S.; Bertrand, D.; Mulley, J.
2007Channelopathies in idiopathic epilepsyHeron, S.; Scheffer, I.; Berkovic, S.; Dibbens, L.; Mulley, J.

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