Adelaide Research & Scholarship
Browsing "School of Molecular and Biomedical Science" by Author Jackson, G.
Showing results 1 to 3 of 3
Preview | Issue Date | Title | Author(s) |
| 2010 | A focal Eeilepsy and intellectual disability syndrome is due to a mutation in TBC1D24 | Bahlo, 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. |
| 2017 | Familial epilepsy with anterior polymicrogyria as a presentation of COL18A1 mutations | Corbett, M.; Turner, S.; Gardner, A.; Silver, J.; Stankovich, J.; Leventer, R.; Derry, C.; Carroll, R.; Ha, T.; Scheffer, I.; Bahlo, M.; Jackson, G.; Mackey, D.; Berkovic, S.; Gecz, J. |
| 2007 | Temporal lobe epilepsy and GEFS(+) phenotypes associated with SCN1B mutations | Scheffer, I.; Harkin, L.; Grinton, B.; Dibbens, L.; Turner, S.; Zielinski, M.; Xu, R.; Jackson, G.; Adams, J.; Connellan, M.; Petrou, S.; Wellard, R.; Briellmann, R.; Wallace, R.; Mulley, J.; Berkovic, S. |