ModelDB: Paper information

Charlier C et al. (1998). A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family. Nature genetics. 18 [PubMed]

See more from authors: Charlier C · Singh NA · Ryan SG · Lewis TB · Reus BE · Leach RJ · Leppert M

References and models cited by this paper

References and models that cite this paper

Miceli F et al. (2013). Genotype-phenotype correlations in neonatal epilepsies caused by mutations in the voltage sensor of K(v)7.2 potassium channel subunits. Proceedings of the National Academy of Sciences of the United States of America. 110 [PubMed]

CA1 pyramidal neuron: effects of R213Q and R312W Kv7.2 mutations (Miceli et al. 2013) [Model]

Miceli F et al. (2015). Early-onset epileptic encephalopathy caused by gain-of-function mutations in the voltage sensor of Kv7.2 and Kv7.3 potassium channel subunits. The Journal of neuroscience : the official journal of the Society for Neuroscience. 35 [PubMed]

Early-onset epileptic encephalopathy (Miceli et al. 2015) [Model]

Miceli F et al. (2009). Neutralization of a unique, negatively-charged residue in the voltage sensor of K V 7.2 subunits in a sporadic case of benign familial neonatal seizures. Neurobiology of disease. 34 [PubMed]

CA1 pyramidal neurons: effects of a Kv7.2 mutation (Miceli et al. 2009) [Model]