UCL Discovery
UCL home » Library Services » Electronic resources » UCL Discovery

Linkage and mutational analysis of CLCN2 in childhood absence epilepsy

Everett, K; Chioza, B; Aicardi, J; Aschauer, H; Brouwer, O; Callenbach, P; Covanis, A; ... Gardiner, M; + view all (2007) Linkage and mutational analysis of CLCN2 in childhood absence epilepsy. EPILEPSY RESEARCH , 75 (2-3) pp. 145-153. 10.1016/j.eplepsyres.2007.05.004. Green open access

[thumbnail of 8217.pdf]
Preview
PDF
8217.pdf

Download (126kB)
Type: Article
Title: Linkage and mutational analysis of CLCN2 in childhood absence epilepsy
Open access status: An open access version is available from UCL Discovery
DOI: 10.1016/j.eplepsyres.2007.05.004
Keywords: Science & Technology, Life Sciences & Biomedicine, Clinical Neurology, Neurosciences & Neurology, childhood absence, epilepsy, linkage, association, mutation screening, CLCN2, IDIOPATHIC GENERALIZED EPILEPSIES, PEDIGREE DISEQUILIBRIUM TEST, GATED CHLORIDE CHANNEL, SELECTIVITY, CELLS, GENE
UCL classification: UCL
URI: https://discovery.ucl.ac.uk/id/eprint/8217
Downloads since deposit
840Downloads
Download activity - last month
Download activity - last 12 months
Downloads by country - last 12 months

Archive Staff Only

View Item View Item