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Neurology, ISSN 0028-3878, 04/2004, Volume 62, Issue 7, pp. 1120 - 1126
Journal Article
Neurology, ISSN 0028-3878, 08/2008, Volume 71, Issue 8, pp. 567 - 571
Journal Article
Epilepsy Research, ISSN 0920-1211, 2014, Volume 108, Issue 5, pp. 972 - 977
Highlights • Mutations in LGI1 cause partial epilepsy with auditory features (PEAF). • Recently a single family with LGI1 microdeletion has been described. •... 
Neurology | LGI1 | MLPA | LTE | Genetic heterogeneity | Microdeletions | PEAF | ADAM22 | LATERAL TEMPORAL EPILEPSY | LT E | CLINICAL NEUROLOGY | GENES | AUTOSOMAL-DOMINANT | ABSENCE | MUTATIONS | DOMINANT PARTIAL EPILEPSY | Sequence Deletion | Humans | Middle Aged | Male | Multiplex Polymerase Chain Reaction | Proteins - genetics | Young Adult | Epilepsy, Partial, Sensory - genetics | DNA Mutational Analysis | Adolescent | Adult | Female | Aged | Epilepsy | Analysis | Medical genetics
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