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Fernández-Marmiesse A, Roca I, Díaz-Flores F, et al. Rare Variants in 48 Genes Account for 42% of Cases of Epilepsy With or Without Neurodevelopmental Delay in 246 Pediatric Patients. Front Neurosci. 2019;13:1135doi: 10.3389/fnins.2019.01135.
Fernández-Marmiesse, A., Roca, I., Díaz-Flores, F., Cantarín, V., Pérez-Poyato, M. S., Fontalba, A., Laranjeira, F., Quintans, S., Moldovan, O., Felgueroso, B., Rodríguez-Pedreira, M., Simón, R., Camacho, A., Quijada, P., Ibanez-Mico, S., Domingno, M. R., Benito, C., Calvo, R., Pérez-Cejas, A., Carrasco, M. L., Ramos, F., Couce, M. L., Ruiz-Falcó, M. L., Gutierrez-Solana, L., & Martínez-Atienza, M. (2019). Rare Variants in 48 Genes Account for 42% of Cases of Epilepsy With or Without Neurodevelopmental Delay in 246 Pediatric Patients. Frontiers in neuroscience, 131135. https://doi.org/10.3389/fnins.2019.01135
Fernández-Marmiesse, Ana, et al. "Rare Variants in 48 Genes Account for 42% of Cases of Epilepsy With or Without Neurodevelopmental Delay in 246 Pediatric Patients." Frontiers in neuroscience vol. 13 (2019): 1135. doi: https://doi.org/10.3389/fnins.2019.01135
Fernández-Marmiesse A, Roca I, Díaz-Flores F, Cantarín V, Pérez-Poyato MS, Fontalba A, Laranjeira F, Quintans S, Moldovan O, Felgueroso B, Rodríguez-Pedreira M, Simón R, Camacho A, Quijada P, Ibanez-Mico S, Domingno MR, Benito C, Calvo R, Pérez-Cejas A, Carrasco ML, Ramos F, Couce ML, Ruiz-Falcó ML, Gutierrez-Solana L, Martínez-Atienza M. Rare Variants in 48 Genes Account for 42% of Cases of Epilepsy With or Without Neurodevelopmental Delay in 246 Pediatric Patients. Front Neurosci. 2019 Nov 08;13:1135. doi: 10.3389/fnins.2019.01135. eCollection 2019. PMID: 31780880; PMCID: PMC6856296.
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