A gain-of-function mutation in the sodium channel gene Scn2a results in seizures and behavioral abnormalities
- 1 January 2001
- journal article
- Published by Elsevier BV in Neuroscience
- Vol. 102 (2), 307-317
- https://doi.org/10.1016/s0306-4522(00)00479-6
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2Nature Genetics, 2000
- Design and construction of a long-term continuous video-EEG monitoring unit for simultaneous recording of multiple small animalsBrain Research Protocols, 1997
- Phenotype variation and newcomers in ion channel disordersHuman Molecular Genetics, 1997
- Genomic Organization of the Mottled Gene, the Mouse Homologue of the Human Menkes Disease GeneGenomics, 1996
- Lidocaine Block of LQT-3 Mutant Human Na + ChannelsCirculation Research, 1996
- Expression of APP in transgenic mice: a Comparison of neuron-specific promotersNeurobiology of Aging, 1996
- Molecular mechanism for an inherited cardiac arrhythmiaNature, 1995
- Mutation of a new sodium channel gene, Scn8a, in the mouse mutant ‘motor endplate disease’Nature Genetics, 1995
- Chapter 25 Expression of Ion Channels by Injection of mRNA into Xenopus OocytesMethods in Cell Biology, 1991
- Transgenic mice expressing β-galactosidase in mature neurons under neuron-specific enolase promoter controlNeuron, 1990