LGI1 microdeletion in autosomal dominant lateral temporal epilepsy

OBJECTIVES: To characterize clinically and genetically a family with autosomal dominant lateral temporal epilepsy (ADLTE) negative to LGI1 exon sequencing test. METHODS: All participants were personally interviewed and underwent neurologic examination. Most affected subjects underwent EEG and neuror...

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Hlavní autoři: Fanciulli, M., Santulli, L., Errichiello, L., Barozzi, C., Tomasi, L., Rigon, L., Cubeddu, T., de Falco, A., Rampazzo, A., Michelucci, R., Uzzau, S., Striano, S., de Falco, F.A., Striano, P., Nobile, C.
Médium: Artigo
Jazyk:Inglês
Vydáno: Lippincott Williams & Wilkins 2012
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3335451/
https://ncbi.nlm.nih.gov/pubmed/22496201
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0b013e3182518328
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