Rare Variants in 48 Genes Account for 42% of Cases of Epilepsy With or Without Neurodevelopmental Delay in 246 Pediatric Patients

AuthID
P-00R-DW1
25
Author(s)
Fernandez Marmiesse, A
·
Roca, I
·
Cantarin, V
·
Socorro Perez Poyato, MS
·
Fontalba, A
·
Laranjeira, F
·
Quintans, S
·
Moldovan, O
·
[+4]·
[+1]·
Benito, C
·
Calvo, R
·
Perez Cejas, A
·
Llanos Carrasco, ML
·
Luz Couce, ML
·
Luz Ruiz Falco, ML
·
Gutierrez Solana, L
·
Martinez Atienza, M
Document Type
Article
Year published
2019
Published
in FRONTIERS IN NEUROSCIENCE, ISSN: 1662-4548
Volume: 13
Indexing
Publication Identifiers
Scopus: 2-s2.0-85075670301
Wos: WOS:000498991200001
Source Identifiers
ISSN: 1662-4548
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Name Order Name   Name Order Name   Name Order Name
1 Fernandez Marmiesse, A;   2 Roca, I;   3 Diaz Flores, F;
4 Cantarin, V;   5 Socorro Perez Poyato, MS;   6 Fontalba, A;
7 Laranjeira, F;   8 Quintans, S;   9 Moldovan, O;
10 Felgueroso, B;   11 Rodriguez Pedreira, M;   12 Simon, R;
13 Camacho, A;   14 Quijada, P;   15 Ibanez Mico, S;
16 Rosario Domingno, MR;   17 Benito, C;   18 Calvo, R;
19 Perez Cejas, A;   20 Llanos Carrasco, ML;   21 Ramos, F;
22 Luz Couce, ML;   23 Luz Ruiz Falco, ML;   24 Gutierrez Solana, L;
25 Martinez Atienza, M;