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Article
2
Female
2
Humans
2
Male
Sanger sequencing
2
disease severity
2
epilepsy
exon
2
family history
2
female
2
gene deletion
2
genetic variability
2
genetics
2
heterozygosity
2
human
2
intellectual impairment
2
male
2
missense mutation
2
mosaicism
2
sequence analysis
2
stop codon
2
ARX gene
1
Argentina
1
Autism Spectrum Disorder
1
Base Sequence
1
Child
1
Child, Preschool
1
Cohort Studies
1
DCX gene
1
DNA Copy Number Variations
1
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1por Nemirovsky, S.I., Córdoba, M., Zaiat, J.J., Completa, S.P., Vega, P.A., González-Morón, D., Medina, N.M., Fabbro, M., Romero, S., Brun, B., Revale, S., Ogara, M.F., Pecci, A., Marti, M., Vazquez, M., Turjanski, A., Kauffman, M.A.Materias: “...epilepsy...”
JOUR -
2por González-Morón, D., Vishnopolska, S., Consalvo, D., Medina, N., Marti, M., Córdoba, M., Vazquez-Dusefante, C., Claverie, S., Rodríguez-Quiroga, S.A., Vega, P., Silva, W., Kochen, S., Kauffman, M.A.Materias: “...epilepsy...”
JOUR