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http://elea.unisa.it/xmlui/handle/10556/4592| Title: | OC.1- Novel CHD2 and KIAA2022 mutations associated with eyelid myoclonia with absences |
| Authors: | Coppola, Antonietta Krithika, Sundararaman Iacomino, Michele Balestrini, Simona Hernandez-Hernandez, Laura Meletti, Stefano Gobbi, Giuseppe Ferlazzo, Edoardo Giordano, Lucio Casellato, Susanna Sofia, Vito Striano, Pasquale Bilo, Leonilda Nigro, Vincenzo Torella, Annalaura Musacchia, Francesco Zara, Federico Sisodiya, Sanjay M. Annual Meeting of the Neapolitan Brain Group 8. <2018 ; Naples> |
| Issue Date: | 2019 |
| 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. |
| URI: | http://www.translationalmedicine.unisa.it/index http://elea.unisa.it:8080/xmlui/handle/10556/4592 http://dx.doi.org/10.14273/unisa-2786 |
| ISSN: | 2239-9747 |
| Appears in Collections: | Translational Medicine @ UniSa. Volume Special Issue 01 2019 |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| 05.pdf | Translational Medicine @ UniSa. Volume Special Issue 01 2019 | 86,59 kB | Adobe PDF | View/Open |
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