TY  - GEN
AU  - Ceulemans,Berten P G M
AU  - Claes,Lieve R F
AU  - Lagae,Lieven G
TI  - Clinical correlations of mutations in the SCN1A gene: from febrile seizures to severe myoclonic epilepsy in infancy
SN  - 0887-8994
PY  - 2004///0802
KW  - Child
KW  - Child, Preschool
KW  - Codon, Nonsense
KW  - genetics
KW  - DNA Mutational Analysis
KW  - Electroencephalography
KW  - Epilepsies, Myoclonic
KW  - diagnosis
KW  - Epilepsy, Generalized
KW  - Exons
KW  - Female
KW  - Frameshift Mutation
KW  - Genotype
KW  - Humans
KW  - Infant
KW  - Intellectual Disability
KW  - Male
KW  - Mutation, Missense
KW  - NAV1.1 Voltage-Gated Sodium Channel
KW  - Nerve Tissue Proteins
KW  - Phenotype
KW  - Seizures, Febrile
KW  - Sodium Channels
KW  - Syndrome
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1016/j.pediatrneurol.2003.10.012
ER  -