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OC.1- Novel CHD2 and KIAA2022 mutations associated with eyelid myoclonia with absences
| dc.contributor.author | Coppola, Antonietta | |
| dc.contributor.author | Krithika, Sundararaman | |
| dc.contributor.author | Iacomino, Michele | |
| dc.contributor.author | Balestrini, Simona | |
| dc.contributor.author | Hernandez-Hernandez, Laura | |
| dc.contributor.author | Meletti, Stefano | |
| dc.contributor.author | Gobbi, Giuseppe | |
| dc.contributor.author | Ferlazzo, Edoardo | |
| dc.contributor.author | Giordano, Lucio | |
| dc.contributor.author | Casellato, Susanna | |
| dc.contributor.author | Sofia, Vito | |
| dc.contributor.author | Striano, Pasquale | |
| dc.contributor.author | Bilo, Leonilda | |
| dc.contributor.author | Nigro, Vincenzo | |
| dc.contributor.author | Torella, Annalaura | |
| dc.contributor.author | Musacchia, Francesco | |
| dc.contributor.author | Zara, Federico | |
| dc.contributor.author | Sisodiya, Sanjay M. | |
| dc.contributor.author | Annual Meeting of the Neapolitan Brain Group 8. <2018 ; Naples> | |
| dc.date.accessioned | 2020-06-26T08:54:34Z | |
| dc.date.available | 2020-06-26T08:54:34Z | |
| dc.date.issued | 2019 | |
| dc.identifier.citation | Coppola 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.issn | 2239-9747 | it_IT |
| dc.identifier.uri | http://www.translationalmedicine.unisa.it/index | it_IT |
| dc.identifier.uri | http://elea.unisa.it:8080/xmlui/handle/10556/4592 | |
| dc.identifier.uri | http://dx.doi.org/10.14273/unisa-2786 | |
| dc.format.extent | P. 5 | it_IT |
| dc.language.iso | en | it_IT |
| dc.source | UniSa. Sistema Bibliotecario di Ateneo | it_IT |
| dc.title | OC.1- Novel CHD2 and KIAA2022 mutations associated with eyelid myoclonia with absences | it_IT |
| dc.type | Article | it_IT |
