SCN1A, SCN2A, and SCN8A are three sodium ion channels found in nerve cells. These channels allow the passage of sodium ions into the cell for proper functioning of actions potentials. This paper considers mutations within these channels that result in epilepsy as well as ataxia, dystonia, and other neurological disorders. Specifically, comparisons are made between these channels to look for patterns, similarities, and differences in these epilepsy-inducing mutations. For instance, the machine-learning tool PolyPhen-2 uses a naïve Bayes approach to assign mutations a pathogenicity score as the posterior probability that the mutation is pathogenic. Trends in these scores are compared across each of the three channels. These patterns are sough...
In excitatory neurons, SCN2A (NaV1.2) and SCN8A (NaV1.6) sodium channels are enriched at the axon in...
The discovery of genetically transmissible form of epilepsy associated with a mutation in a gene tha...
Epilepsies are the results of abnormal brain hyperactivities caused by brain injury, drug intoxicati...
Genetic epilepsy occurs as a result of mutations in either a single gene or an interplay of differen...
Voltage-gated sodium ion channels play a vital role in neuron function, which becomes evident when v...
International audienceObjectiveVoltage‐gated sodium channels (SCNs) share similar amino acid sequenc...
While most cases of epilepsy respond well to common antiepileptic drugs, many genetically-driven epi...
Variants implicated in childhood epilepsy have been identified in all four voltage-gated sodium chan...
The number of mutations in the voltage-gated sodium channel Nav1.1, encoded by SCN1A, that have been...
The human sodium channel family includes seven neuronal channels that are essential for the initiati...
Over 1250 mutations in SCN1A, the Nav1.1 voltage-gated sodium channel gene, are associated with a va...
identified in families with generalized epilepsy with febrile seizures plus (GEFS+). A novel mutatio...
Mutations in the SCN1A gene, which encodes for the voltage-gated sodium channel NaV1.1, cause Dravet...
BACKGROUND: Mutations of SCN8A encoding the neuronal voltage-gated sodium channel NaV1.6 are associa...
Background: Mutations of SCN8A encoding the neuronal voltage-gated sodium channel NaV1.6 are associa...
In excitatory neurons, SCN2A (NaV1.2) and SCN8A (NaV1.6) sodium channels are enriched at the axon in...
The discovery of genetically transmissible form of epilepsy associated with a mutation in a gene tha...
Epilepsies are the results of abnormal brain hyperactivities caused by brain injury, drug intoxicati...
Genetic epilepsy occurs as a result of mutations in either a single gene or an interplay of differen...
Voltage-gated sodium ion channels play a vital role in neuron function, which becomes evident when v...
International audienceObjectiveVoltage‐gated sodium channels (SCNs) share similar amino acid sequenc...
While most cases of epilepsy respond well to common antiepileptic drugs, many genetically-driven epi...
Variants implicated in childhood epilepsy have been identified in all four voltage-gated sodium chan...
The number of mutations in the voltage-gated sodium channel Nav1.1, encoded by SCN1A, that have been...
The human sodium channel family includes seven neuronal channels that are essential for the initiati...
Over 1250 mutations in SCN1A, the Nav1.1 voltage-gated sodium channel gene, are associated with a va...
identified in families with generalized epilepsy with febrile seizures plus (GEFS+). A novel mutatio...
Mutations in the SCN1A gene, which encodes for the voltage-gated sodium channel NaV1.1, cause Dravet...
BACKGROUND: Mutations of SCN8A encoding the neuronal voltage-gated sodium channel NaV1.6 are associa...
Background: Mutations of SCN8A encoding the neuronal voltage-gated sodium channel NaV1.6 are associa...
In excitatory neurons, SCN2A (NaV1.2) and SCN8A (NaV1.6) sodium channels are enriched at the axon in...
The discovery of genetically transmissible form of epilepsy associated with a mutation in a gene tha...
Epilepsies are the results of abnormal brain hyperactivities caused by brain injury, drug intoxicati...