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Carboxypeptidase A6 gene (CPA6) mutations in a recessive familial form of febrile seizures and temporal lobe epilepsy and in sporadic temporal lobe epilepsy.
Salzmann A, Guipponi M, Lyons PJ, Fricker LD, Sapio M, Lambercy C, Buresi C, Ouled Amar Bencheikh B, Lahjouji F, Ouazzani R, Crespel A, Chaigne D, Malafosse A. Salzmann A, et al. Among authors: guipponi m. Hum Mutat. 2012 Jan;33(1):124-35. doi: 10.1002/humu.21613. Epub 2011 Oct 31. Hum Mutat. 2012. PMID: 21922598
Association of the connexin36 gene with juvenile myoclonic epilepsy.
Mas C, Taske N, Deutsch S, Guipponi M, Thomas P, Covanis A, Friis M, Kjeldsen MJ, Pizzolato GP, Villemure JG, Buresi C, Rees M, Malafosse A, Gardiner M, Antonarakis SE, Meda P. Mas C, et al. Among authors: guipponi m. J Med Genet. 2004 Jul;41(7):e93. doi: 10.1136/jmg.2003.017954. J Med Genet. 2004. PMID: 15235036 Free PMC article. No abstract available.
15q13.3 microdeletions increase risk of idiopathic generalized epilepsy.
Helbig I, Mefford HC, Sharp AJ, Guipponi M, Fichera M, Franke A, Muhle H, de Kovel C, Baker C, von Spiczak S, Kron KL, Steinich I, Kleefuss-Lie AA, Leu C, Gaus V, Schmitz B, Klein KM, Reif PS, Rosenow F, Weber Y, Lerche H, Zimprich F, Urak L, Fuchs K, Feucht M, Genton P, Thomas P, Visscher F, de Haan GJ, Møller RS, Hjalgrim H, Luciano D, Wittig M, Nothnagel M, Elger CE, Nürnberg P, Romano C, Malafosse A, Koeleman BP, Lindhout D, Stephani U, Schreiber S, Eichler EE, Sander T. Helbig I, et al. Among authors: guipponi m. Nat Genet. 2009 Feb;41(2):160-2. doi: 10.1038/ng.292. Epub 2009 Jan 11. Nat Genet. 2009. PMID: 19136953 Free PMC article.
115 results