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dc.contributor.authorCoppola, Antonietta
dc.contributor.authorKrithika, Sundararaman
dc.contributor.authorIacomino, Michele
dc.contributor.authorBalestrini, Simona
dc.contributor.authorHernandez-Hernandez, Laura
dc.contributor.authorMeletti, Stefano
dc.contributor.authorGobbi, Giuseppe
dc.contributor.authorFerlazzo, Edoardo
dc.contributor.authorGiordano, Lucio
dc.contributor.authorCasellato, Susanna
dc.contributor.authorSofia, Vito
dc.contributor.authorStriano, Pasquale
dc.contributor.authorBilo, Leonilda
dc.contributor.authorNigro, Vincenzo
dc.contributor.authorTorella, Annalaura
dc.contributor.authorMusacchia, Francesco
dc.contributor.authorZara, Federico
dc.contributor.authorSisodiya, Sanjay M.
dc.contributor.authorAnnual Meeting of the Neapolitan Brain Group 8. <2018 ; Naples>
dc.date.accessioned2020-06-26T08:54:34Z
dc.date.available2020-06-26T08:54:34Z
dc.date.issued2019
dc.identifier.citationCoppola A, Krithika S, Iacomino M, Balestrini S, Hernandez-Hernandez L, Meletti S, Gobbi G, Ferlazzo E, Giordano L, Casellato S, Sofia V, Striano P, Bilo L, Nigro V, Torella A, Musacchia F, Zara F, Sisodiya SM. OC.1- Novel CHD2 and KIAA2022 mutations associated with eyelid myoclonia with absences. [oral communications presentata a: 8th Annual Meeting of the Neapolitan Brain Group, Naples, 13 December 2018]. Translational Medicine @ UniSa. Volume Special Issue 1(2019): 5.it_IT
dc.identifier.issn2239-9747it_IT
dc.identifier.urihttp://www.translationalmedicine.unisa.it/indexit_IT
dc.identifier.urihttp://elea.unisa.it:8080/xmlui/handle/10556/4592
dc.format.extentP. 5it_IT
dc.language.isoenit_IT
dc.sourceUniSa. Sistema Bibliotecario di Ateneoit_IT
dc.titleOC.1- Novel CHD2 and KIAA2022 mutations associated with eyelid myoclonia with absencesit_IT
dc.typeArticleit_IT
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