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Epilepsy Research Centre and Department of Medicine (Neurology), University of Melbourne | 論文
- Clinical and molecular genetics of myoclonic-astatic epilepsy and severe myoclonic epilepsy in infancy (Dravet syndrome)
- Familial Partial Epilepsy with Variable Foci : Clinical Features and Linkage to Chromosome 22q12
- Genetic Architecture of Idiopathic Generalized Epilepsy : Clinical Genetic Analysis of 55 Multiplex Families
- Is Variation in the GABA(B) Receptor 1 Gene Associated with Temporal Lobe Epilepsy?
- Genetic Association Studies in Epilepsy : "The Truth Is Out There"
- Febrile Convulsions and Genetic Susceptibility : Role of the Neuronal Nicotinic Acetylcholine Receptor α4 Subunit
- Genetics of the Epilepsies