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Heterozygous Reelin Mutations Cause Autosomal-Dominant Lateral Temporal Epilepsy
Autosomal-dominant lateral temporal epilepsy (ADLTE) is a genetic epilepsy syndrome clinically characterized by focal seizures with prominent auditory symptoms. ADLTE is genetically heterogeneous, and mutations in LGI1 account for fewer than 50% of affected families. Here, we report the identificati...
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Publicado no: | Am J Hum Genet |
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Main Authors: | , , , , , , , , , , , , , , , , , , , , , , |
Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
Elsevier
2015
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4457960/ https://ncbi.nlm.nih.gov/pubmed/26046367 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2015.04.020 |
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