What's new in epilepsy genetics?
- 1 May 2003
- journal article
- review article
- Published by Springer Nature in Molecular Psychiatry
- Vol. 8 (5) , 463-465
- https://doi.org/10.1038/sj.mp.4001292
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- A nonsense mutation of the MASS1 gene in a family with febrile and afebrile seizuresAnnals of Neurology, 2002
- Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory featuresNature Genetics, 2002
- Very Large G Protein-coupled Receptor-1, the Largest Known Cell Surface Protein, Is Highly Expressed in the Developing Central Nervous SystemJournal of Biological Chemistry, 2002
- A Novel Gene Causing a Mendelian Audiogenic Mouse EpilepsyNeuron, 2001
- Sequence Similarities between a Novel Putative G Protein-Coupled Receptor and Na+/Ca2+ Exchangers Define a Cation Binding DomainMolecular Endocrinology, 2000
- Paroxysmal kinesigenic dyskinesia and infantile convulsionsNeurology, 2000
- Calx, a Na-Ca exchanger gene ofDrosophila melanogasterProceedings of the National Academy of Sciences, 1997
- Andersen's syndrome: A distinct periodic paralysisAnnals of Neurology, 1997
- A Met-to-Val mutation in the skeletal muscle Na+ channel α-subunit in hyperkalaemic periodic paralysisNature, 1991
- Identification of a mutation in the gene causing hyperkalemic periodic paralysisCell, 1991