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

par 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 G;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;Sanders, J.;Duncan, John S;Scheffer, Ingrid E;Berkovic, S F;Wood, Nicholas W;Doherty, Colin P;Delanty, Norman;Sisodiya, Sanjay M;Goldstein, David B
Référence Lancet neurology, 6, 11, page (970-980)
Publication Publié, 2007-11

Article révisé par les pairs

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Titre:	Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study.
Auteur:	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 G; 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; Sanders, J.; Duncan, John S; Scheffer, Ingrid E; Berkovic, S F; Wood, Nicholas W; Doherty, Colin P; Delanty, Norman; Sisodiya, Sanjay M; Goldstein, David B
Informations sur la publication:	Lancet neurology, 6, 11, page (970-980)
Statut de publication:	Publié, 2007-11
Sujet CREF:	Sciences bio-médicales et agricoles
MeSH keywords:	Adult
	Case-Control Studies
	Chromosome Mapping
	Cohort Studies
	Epilepsy -- genetics
	Genetic Predisposition to Disease
	Genetic Variation
	Genotype
	Humans
	Kv1.3 Potassium Channel -- genetics
	Large-Conductance Calcium-Activated Potassium Channel beta Subunits -- genetics
	Nerve Tissue Proteins -- genetics
	Phenotype
	Polymorphism, Single Nucleotide
	Receptors, GABA-B -- genetics
	Seizures -- genetics
	Succinate-Semialdehyde Dehydrogenase -- genetics
	Synapsins -- genetics
	Syndrome
Note générale:	Journal Article
	Multicenter Study
	Research Support, Non-U.S. Gov't
	SCOPUS: ar.j
Langue:	Anglais
Identificateurs:	urn:issn:1474-4422
	info:doi/10.1016/S1474-4422(07)70247-8
	info:pii/S1474-4422(07)70247-8
	info:scp/35248883597
	info:pmid/17913586