Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study

The Epilepsy Genetics (EPIGEN) Consortium was established to undertake genetic mapping analyses with augmented statistical power to detect variants that influence the development and treatment of common forms of epilepsy.

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Veröffentlicht in:The Lancet Neurology 2007-11, Vol.6 (11), p.970-980
Hauptverfasser: Cavalleri, Gianpiero L, Weale, Michael E, Shianna, Kevin V, Singh, Rinki, Lynch, John M, Grinton, Bronwyn, Szoeke, Cassandra, Murphy, Kevin, Kinirons, Peter, O'Rourke, Deirdre, Ge, Dongliang, Depondt, Chantal, Claeys, Kristl, Pandolfo, Massimo, Gumbs, Curtis, Walley, Nicole, McNamara, James, Mulley, John C, Linney, Kristen N, Sheffield, Leslie J, Radtke, Rodney A, Tate, Sarah K, Chissoe, Stephanie L, Gibson, Rachel A, Hosford, David, Stanton, Alice, Graves, Tracey D, Hanna, Michael G, Eriksson, Kai, Kantanen, Anne-Mari, Kalviainen, Reetta, O'Brien, Terence J, Sander, Josemir W, Duncan, John S, Scheffer, Ingrid E, Berkovic, Samuel F, Wood, Nicholas W, Doherty, Colin P, Delanty, Norman, Sisodiya, Sanjay M, Goldstein, David B
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Sprache:eng
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Zusammenfassung:The Epilepsy Genetics (EPIGEN) Consortium was established to undertake genetic mapping analyses with augmented statistical power to detect variants that influence the development and treatment of common forms of epilepsy.
ISSN:1474-4422