No abstract available
MeSH terms
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Child, Preschool
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Epilepsies, Myoclonic / genetics
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Epilepsy, Benign Neonatal / diagnosis
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Epilepsy, Benign Neonatal / genetics*
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Epilepsy, Generalized / diagnosis
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Epilepsy, Generalized / genetics*
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Female
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Genetic Heterogeneity
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Humans
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Infant
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KCNQ2 Potassium Channel / genetics
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KCNQ3 Potassium Channel / genetics
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Male
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Mutation
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NAV1.1 Voltage-Gated Sodium Channel
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Nerve Tissue Proteins / genetics
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Phenotype
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Receptors, GABA-A / genetics
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Receptors, GABA-B / genetics
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Seizures, Febrile / diagnosis
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Seizures, Febrile / genetics*
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Sodium Channels / genetics
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Voltage-Gated Sodium Channel beta-1 Subunit
Substances
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GABRD protein, human
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GABRR2 protein, human
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KCNQ2 Potassium Channel
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KCNQ2 protein, human
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KCNQ3 Potassium Channel
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NAV1.1 Voltage-Gated Sodium Channel
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Nerve Tissue Proteins
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Receptors, GABA-A
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Receptors, GABA-B
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SCN1A protein, human
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SCN1B protein, human
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Sodium Channels
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Voltage-Gated Sodium Channel beta-1 Subunit