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Evaluation of the positional candidate gene CHRNA7 at the juvenile myoclonic epilepsy locus (EJM2) on chromosome 15q13-14.
Taske NL, Williamson MP, Makoff A, Bate L, Curtis D, Kerr M, Kjeldsen MJ, Pang KA, Sundqvist A, Friis ML, Chadwick D, Richens A, Covanis A, Santos M, Arzimanoglou A, Panayiotopoulos CP, Whitehouse WP, Rees M, Gardiner RM. Taske NL, et al. Among authors: whitehouse wp. Epilepsy Res. 2002 Apr;49(2):157-72. doi: 10.1016/s0920-1211(02)00027-x. Epilepsy Res. 2002. PMID: 12049804
Linkage analysis of idiopathic generalised epilepsy in families of probands with Juvenile Myoclonic Epilepsy and marker loci in the region of EPM 1 on chromosome 21 q: Unverricht-Lundborg disease and JME are not allelic variants.
Rees M, Curtis D, Parker K, Sundqvist A, Baralle D, Bespalova IN, Burmeister M, Chung E, Gardiner RM, Whitehouse WP. Rees M, et al. Among authors: whitehouse wp. Neuropediatrics. 1994 Feb;25(1):20-5. doi: 10.1055/s-2008-1071576. Neuropediatrics. 1994. PMID: 8208346
Linkage analysis of juvenile myoclonic epilepsy and microsatellite loci spanning 61 cM of human chromosome 6p in 19 nuclear pedigrees provides no evidence for a susceptibility locus in this region.
Elmslie FV, Williamson MP, Rees M, Kerr M, Kjeldsen MJ, Pang KA, Sundqvist A, Friis ML, Richens A, Chadwick D, Whitehouse WP, Gardiner RM. Elmslie FV, et al. Among authors: whitehouse wp. Am J Hum Genet. 1996 Sep;59(3):653-63. Am J Hum Genet. 1996. PMID: 8751867 Free PMC article.
Linkage analysis between childhood absence epilepsy and genes encoding GABAA and GABAB receptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8q.
Robinson R, Taske N, Sander T, Heils A, Whitehouse W, Goutières F, Aicardi J, Lehesjoki AE, Siren A, Laue Friis M, Kjeldsen MJ, Panayiotopoulos C, Kennedy C, Ferrie C, Rees M, Gardiner RM. Robinson R, et al. Epilepsy Res. 2002 Feb;48(3):169-79. doi: 10.1016/s0920-1211(01)00335-7. Epilepsy Res. 2002. PMID: 11904235
121 results