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MeSH Review

Epilepsy, Temporal Lobe

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Disease relevance of Epilepsy, Temporal Lobe


  1. Autosomal dominant lateral temporal epilepsy: two families with novel mutations in the LGI1 gene. Hedera, P., Abou-Khalil, B., Crunk, A.E., Taylor, K.A., Haines, J.L., Sutcliffe, J.S. Epilepsia (2004) [Pubmed]
  2. Familial partial epilepsy with variable foci in a Dutch family: clinical characteristics and confirmation of linkage to chromosome 22q. Callenbach, P.M., van den Maagdenberg, A.M., Hottenga, J.J., van den Boogerd, E.H., de Coo, R.F., Lindhout, D., Frants, R.R., Sandkuijl, L.A., Brouwer, O.F. Epilepsia (2003) [Pubmed]
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