1. Elea
  2. Dipartimenti e Centri di ricerca UniSA. Pubblicazioni scientifiche
  3. Translational Medicine @ UniSa
  4. Translational Medicine @ UniSa. Volume Special Issue 01 2019
Utilizza questo identificativo per citare o creare un link a questo documento: http://elea.unisa.it/xmlui/handle/10556/4592
Record completo di tutti i metadati
Campo DCValoreLingua
dcterms.contributor.authorCoppola, Antonietta
dcterms.contributor.authorKrithika, Sundararaman
dcterms.contributor.authorIacomino, Michele
dcterms.contributor.authorBalestrini, Simona
dcterms.contributor.authorHernandez-Hernandez, Laura
dcterms.contributor.authorMeletti, Stefano
dcterms.contributor.authorGobbi, Giuseppe
dcterms.contributor.authorFerlazzo, Edoardo
dcterms.contributor.authorGiordano, Lucio
dcterms.contributor.authorCasellato, Susanna
dcterms.contributor.authorSofia, Vito
dcterms.contributor.authorStriano, Pasquale
dcterms.contributor.authorBilo, Leonilda
dcterms.contributor.authorNigro, Vincenzo
dcterms.contributor.authorTorella, Annalaura
dcterms.contributor.authorMusacchia, Francesco
dcterms.contributor.authorZara, Federico
dcterms.contributor.authorSisodiya, Sanjay M.
dcterms.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
dcterms.date.issued2019
dcterms.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
dcterms.identifier.issn2239-9747it_IT
dcterms.identifier.urihttp://www.translationalmedicine.unisa.it/indexit_IT
dcterms.identifier.urihttp://elea.unisa.it:8080/xmlui/handle/10556/4592
dcterms.identifier.urihttp://dx.doi.org/10.14273/unisa-2786-
dcterms.format.extentP. 5it_IT
dc.language.isoenit_IT
dcterms.sourceUniSa. Sistema Bibliotecario di Ateneoit_IT
dcterms.titleOC.1- Novel CHD2 and KIAA2022 mutations associated with eyelid myoclonia with absencesit_IT
dcterms.typeArticleit_IT
È visualizzato nelle collezioni:Translational Medicine @ UniSa. Volume Special Issue 01 2019

File in questo documento:
File Descrizione DimensioniFormato 
Translational Medicine 2019.pdfTranslational Medicine @ UniSa. Volume Special Issue 01 201986,59 kBAdobe PDFVisualizza/apri
Visualizza la scheda semplice del documento SFX Query


Tutti i documenti archiviati in DSpace sono protetti da copyright. Tutti i diritti riservati.