Mutation screen of the GABAA receptor gamma 2 subunit gene in Chinese patients with childhood absence epilepsy
- 31 October 2002
- journal article
- clinical trial
- Published by Elsevier BV in Neuroscience Letters
- Vol. 332 (2), 75-78
- https://doi.org/10.1016/s0304-3940(02)00805-4
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Truncation of the GABAA-Receptor γ2 Subunit in a Family with Generalized Epilepsy with Febrile Seizures PlusAmerican Journal of Human Genetics, 2002
- First genetic evidence of GABAA receptor dysfunction in epilepsy: a mutation in the γ2-subunit geneNature Genetics, 2001
- Mutant GABAA receptor γ2-subunit in childhood absence epilepsy and febrile seizuresNature Genetics, 2001
- The ‘ABC’ of GABA receptorsTrends in Pharmacological Sciences, 2000
- Mechanisms of generalized absence epilepsyBrain & Development, 1998
- Basic mechanisms of generalized absence seizuresAnnals of Neurology, 1995
- Genetic Dissection of Complex TraitsScience, 1994
- Proposal for Revised Classification of Epilepsies and Epileptic SyndromesEpilepsia, 1989
- A simple salting out procedure for extracting DNA from human nucleated cellsNucleic Acids Research, 1988
- Concepts of absence epilepsiesNeurology, 1987