Open AccessTwo Novel Epilepsy-Linked Mutations Leading to a Loss of Function of LGI1
Author(s) -
E Chabrol,
Cyprian Popescu,
Isabelle GourfinkelAn,
Oriane Trouillard,
Christel Depienne,
Kristen Senechal,
Michel Baulac,
Eric Leguern,
Stéphanie Baulac
Publication year - 2007
Publication title -
archives of neurology
Language(s) - English
Resource type - Journals
eISSN - 1538-3687
pISSN - 0003-9942
DOI - 10.1001/archneur.64.2.217
Subject(s) - epilepsy , mutation , exon , mutant , genetics , biology , loss function , phenotype , gene , neuroscience
Mutations in the leucine-rich, glioma-inactivated 1 (LGI1) gene have been implicated in autosomal dominant lateral temporal epilepsy.
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