Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: KCNMB4[original query] |
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Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study. The Lancet. Neurology 2007 Nov 6 (11): 970-80. 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, 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 |
Failure to confirm association of a polymorphism in KCNMB4 gene with mesial temporal lobe epilepsy. Epilepsy research 2013 Sep 106 (1-2): 284-7. Manna Ida, Labate Angelo, Mumoli Laura, Ferlazzo Edoardo, Aguglia Umberto, Quattrone Aldo, Gambardella Anton |
Family-Based Cohort Association Study of PRKCB1, CBLN1 and KCNMB4 Gene Polymorphisms and Autism in Polish Population. Journal of autism and developmental disorders 2021 Sep . Iwanicki Tomasz, Balcerzyk Anna, Kazek Beata, Emich-Widera Ewa, Likus Wirginia, Iwanicka Joanna, Kapinos-Gorczyca Agnieszka, Kapinos Maciej, Jarosz Alicja, Grzeszczak W?adys?aw, Górczy?ska-Kosiorz Sylwia, Niemiec Paw |
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