Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.410 |
GeneticVariation
|
group |
CLINVAR |
The spectrum of SCN1A-related infantile epileptic encephalopathies.
|
17347258 |
2007 |
Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.410 |
GeneticVariation
|
group |
CLINVAR |
Somatic and germline mosaicisms in severe myoclonic epilepsy of infancy.
|
16430863 |
2006 |
Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.410 |
GeneticVariation
|
group |
CLINVAR |
Timing of de novo mutagenesis--a twin study of sodium-channel mutations.
|
20879882 |
2010 |
Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.410 |
CausalMutation
|
group |
CLINVAR |
Timing of de novo mutagenesis--a twin study of sodium-channel mutations.
|
20879882 |
2010 |
Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.410 |
CausalMutation
|
group |
CLINVAR |
SCN1A duplications and deletions detected in Dravet syndrome: implications for molecular diagnosis.
|
19400878 |
2009 |
Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.410 |
GeneticVariation
|
group |
CLINVAR |
Structure and function of voltage-gated sodium channels at atomic resolution.
|
24097157 |
2014 |
Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.410 |
GeneticVariation
|
group |
CLINVAR |
Genotype-phenotype associations in SCN1A-related epilepsies.
|
21248271 |
2011 |
Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.410 |
CausalMutation
|
group |
CLINVAR |
Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2.
|
10742094 |
2000 |
Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.410 |
CausalMutation
|
group |
CLINVAR |
Cognitive development in Dravet syndrome: a retrospective, multicenter study of 26 patients.
|
21269283 |
2011 |
Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.410 |
GeneticVariation
|
group |
CLINVAR |
Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome.
|
22719002 |
2012 |
Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.410 |
CausalMutation
|
group |
CLINVAR |
Somatic and germline mosaicisms in severe myoclonic epilepsy of infancy.
|
16430863 |
2006 |
Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.410 |
CausalMutation
|
group |
CLINVAR |
Severe myoclonic epilepsy in infancy: Dravet syndrome.
|
15508915 |
2005 |
Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.410 |
GeneticVariation
|
group |
CLINVAR |
Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2.
|
10742094 |
2000 |
Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.410 |
GeneticVariation
|
group |
CLINVAR |
Cognitive development in Dravet syndrome: a retrospective, multicenter study of 26 patients.
|
21269283 |
2011 |
Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.410 |
CausalMutation
|
group |
CLINVAR |
Idiopathic epilepsies with seizures precipitated by fever and SCN1A abnormalities.
|
17561957 |
2007 |
Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.410 |
CausalMutation
|
group |
CLINVAR |
Structure and function of voltage-gated sodium channels at atomic resolution.
|
24097157 |
2014 |