F. Bisulli, P. Tinuper, C. Marini, P. Avoni, G. Carraro et al., Partial epilepsy with prominent auditory symptoms not linked to chromosome 10q, Epileptic Disord, vol.4, pp.183-187, 2002.

F. Bisulli, P. Tinuper, E. Scudellaro, I. Naldi, A. Bagattin et al., A de novo LGI1 mutation in sporadic partial epilepsy with auditory features, Annals of Neurology, vol.44, issue.3, pp.455-456, 2004.
DOI : 10.1002/ana.20218

E. Brodtkorb, W. Gu, K. O. Nakken, C. Fischer, and O. K. Steinlein, Familial Temporal Lobe Epilepsy with Aphasic Seizures and Linkage to Chromosome 10q22-q24, Epilepsia, vol.43, issue.3, pp.228-235, 2002.
DOI : 10.1046/j.1528-1157.2002.32001.x

E. Brodtkorb, R. P. Michler, W. Gu, and O. K. Steinlein, Speech-induced Aphasic Seizures in Epilepsy Caused by LGI1 Mutation, Epilepsia, vol.41, issue.6, pp.963-966, 2005.
DOI : 10.1001/archneur.60.11.1546

E. Chabrol, C. Popescu, I. Gourfinkel-an, O. Trouillard, C. Depienne et al., Two Novel Epilepsy-Linked Mutations Leading to a Loss of Function of LGI1, Archives of Neurology, vol.64, issue.2, pp.217-222, 2007.
DOI : 10.1001/archneur.64.2.217
URL : https://hal.archives-ouvertes.fr/inserm-00306475

E. Fertig, A. Lincoln, A. Martinuzzi, R. H. Mattson, and F. M. Hisama, Novel LGI1 mutation in a family with autosomal dominant partial epilepsy with auditory features, Neurology, vol.60, issue.10, 2003.
DOI : 10.1212/01.WNL.0000063324.39980.4A

Y. Fukata, H. Adesnik, T. Iwanaga, D. S. Bredt, R. A. Nicoll et al., Epilepsy-Related Ligand/Receptor Complex LGI1 and ADAM22 Regulate Synaptic Transmission, Science, vol.313, issue.5794, pp.1792-1795, 2006.
DOI : 10.1126/science.1129947

W. Gu, E. Brodtkorb, and O. K. Steinlein, LGI1 is mutated in familial temporal lobe epilepsy characterized by aphasic seizures, Annals of Neurology, vol.265, issue.3, pp.364-367, 2002.
DOI : 10.1002/ana.10280

W. Gu, A. Wevers, H. Schroder, K. H. Grzeschik, C. Derst et al., The LGI1 gene involved in lateral temporal lobe epilepsy belongs to a new subfamily of leucine-rich repeat proteins, FEBS Letters, vol.8, issue.1-3, pp.71-76, 2002.
DOI : 10.1016/S0014-5793(02)02713-8

W. A. Hauser, The Prevalence and Incidence of Convulsive Disorders in Children, Epilepsia, vol.110, issue.s2, pp.1-6, 1994.
DOI : 10.1203/00006450-196907000-00005

P. Hedera, B. Abou-khalil, A. E. Crunk, K. A. Taylor, J. L. Haines et al., Autosomal Dominant Lateral Temporal Epilepsy: Two Families with Novel Mutations in the LGI1 Gene, Epilepsia, vol.60, issue.1, pp.218-222, 2004.
DOI : 10.1093/hmg/11.15.1757

A. Ikeda, T. Kunieda, S. Miyamoto, H. Fukuyama, and H. Shibasaki, Autosomal dominant temporal lobe epilepsy in a Japanese family, Journal of the Neurological Sciences, vol.176, issue.2, pp.162-165, 2000.
DOI : 10.1016/S0022-510X(00)00333-6

S. Kalachikov, O. Evgrafov, B. Ross, M. Winawer, C. Barker-cummings et al., Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features, Nature Genetics, vol.30, issue.3, pp.335-341, 2002.
DOI : 10.1038/ng832

E. Kobayashi, N. F. Santos, F. R. Torres, R. Secolin, L. A. Sardinha et al., Magnetic Resonance Imaging Abnormalities in Familial Temporal Lobe Epilepsy With Auditory Auras, Archives of Neurology, vol.60, issue.11, pp.1546-1551, 2003.
DOI : 10.1001/archneur.60.11.1546

R. Michelucci, J. J. Poza, V. Sofia, M. R. De-feo, S. Binelli et al., Autosomal Dominant Lateral Temporal Epilepsy: Clinical Spectrum, New Epitempin Mutations, and Genetic Heterogeneity in Seven European Families, Epilepsia, vol.5, issue.suppl 5, 2003.
DOI : 10.1046/j.1528-1157.2003.20003.x

R. Ottman, N. Risch, W. A. Hauser, T. A. Pedley, J. H. Lee et al., Localization of a gene for partial epilepsy to chromosome 10q, Nature Genetics, vol.17, issue.1, pp.56-60, 1995.
DOI : 10.1016/S0140-6736(94)91463-X

T. Pisano, C. Marini, P. Brovedani, D. Brizzolara, D. Pruna et al., Abnormal Phonologic Processing in Familial Lateral Temporal Lobe Epilepsy Due to a New LGI1 Mutation, Epilepsia, vol.47, issue.8, pp.118-123, 2005.
DOI : 10.1055/s-2003-43255

A. Pizzuti, E. Flex, D. Bonaventura, C. Dottorini, T. Egeo et al., Epilepsy with auditory features: ALGI1 gene mutation suggests a loss-of-function mechanism, Annals of Neurology, vol.390, issue.3, pp.396-399, 2003.
DOI : 10.1002/ana.10492

J. J. Poza, A. Saenz, A. Martinez-gil, N. Cheron, A. M. Cobo et al., Autosomal dominant lateral temporal epilepsy: Clinical and genetic study of a large basque pedigree linked to chromosome 10q, Annals of Neurology, vol.38, issue.2, pp.182-188, 1999.
DOI : 10.1002/1531-8249(199902)45:2<182::AID-ANA8>3.0.CO;2-G

K. Sagane, K. Hayakawa, J. Kai, T. Hirohashi, E. Takahashi et al., Ataxia and peripheral nerve hypomyelination in ADAM22-deficient mice, BMC Neuroscience, vol.6, issue.1, p.33, 2005.
DOI : 10.1186/1471-2202-6-33

M. R. Winawer, M. Boneschi, F. Barker-cummings, C. Lee, J. H. Liu et al., Four New Families with Autosomal Dominant Partial Epilepsy with Auditory Features: Clinical Description and Linkage to Chromosome 10q24, Epilepsia, vol.11, issue.1, pp.60-67, 2002.
DOI : 10.1046/j.1528-1157.2002.45001.x

M. R. Winawer, R. Ottman, W. A. Hauser, and T. A. Pedley, Autosomal dominant partial epilepsy with auditory features: Defining the phenotype, Neurology, vol.54, issue.11, pp.2173-2176, 2000.
DOI : 10.1212/WNL.54.11.2173