Association of the connexin36 gene with juvenile myoclonic epilepsy. Issue 7 (2nd July 2004)

• Record Type: Journal Article
• Authors: Mas, C; Taske, N; Deutsch, S; Guipponi, M; Thomas, P; Covanis, A; Friis, M; Kjeldsen, M J; Pizzolato, G P; Villemure, J-G; Buresi, C; Rees, M; Malafosse, A; Gardiner, M; Antonarakis, S E; Meda, P
• Is Part Of: Journal of medical genetics. Volume 41:Issue 7(2004)
• Page Start: e93
• Page End: e93
• Publication Date: 2004-07-02
• Subjects: CEPH, Centre d'Etude du Polymorphisme Humain -- ESE, exonic splicing enhancer -- HW, Hardy-Weinberg -- ILAE, International League Against Epilepsy -- JME, juvenile myoclonic epilepsy -- LD, linkage disequilibrium -- RS, randomly selected -- SNP, single nucleotide polymorphism; connexin36 -- gap junction -- idiopathic epilepsy -- juvenile myoclonic epilepsy -- single nucleotide polymorphism; Medical genetics -- Periodicals; 616.042
• DOI: 10.1136/jmg.2003.017954
• Languages: English
• ISSNs: 1468-6244