Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.800 |
GeneticVariation
|
disease |
CLINVAR |
|
|
|
Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.800 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
|
|
|
Entrez Id: |
81609 |
Gene Symbol: |
SNX27 |
SNX27
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
|
|
|
SCN1A-AS1
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
|
|
|
Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.800 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2.
|
10742094 |
2000 |
Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.800 |
GeneticVariation
|
disease |
UNIPROT |
De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy.
|
11359211 |
2001 |
Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.800 |
CausalMutation
|
disease |
CLINVAR |
De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy.
|
11359211 |
2001 |
SCN1A-AS1
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy.
|
11359211 |
2001 |
Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.800 |
CausalMutation
|
disease |
CLINVAR |
Significant correlation of the SCN1A mutations and severe myoclonic epilepsy in infancy.
|
12083760 |
2002 |
Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.800 |
GeneticVariation
|
disease |
UNIPROT |
Significant correlation of the SCN1A mutations and severe myoclonic epilepsy in infancy.
|
12083760 |
2002 |
Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.800 |
CausalMutation
|
disease |
CLINVAR |
Frequent mutations of SCN1A in severe myoclonic epilepsy in infancy.
|
11940708 |
2002 |
SCN1A-AS1
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
Significant correlation of the SCN1A mutations and severe myoclonic epilepsy in infancy.
|
12083760 |
2002 |
SCN1A-AS1
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
Frequent mutations of SCN1A in severe myoclonic epilepsy in infancy.
|
11940708 |
2002 |
Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.800 |
CausalMutation
|
disease |
CLINVAR |
Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy.
|
12821740 |
2003 |
Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.800 |
GeneticVariation
|
disease |
UNIPROT |
De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy.
|
12754708 |
2003 |
Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.800 |
GeneticVariation
|
disease |
UNIPROT |
Epilepsy-associated dysfunction in the voltage-gated neuronal sodium channel SCN1A.
|
14672992 |
2003 |
Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.800 |
CausalMutation
|
disease |
CLINVAR |
De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy.
|
12754708 |
2003 |
Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.800 |
GeneticVariation
|
disease |
UNIPROT |
Mutations of sodium channel alpha subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures.
|
12566275 |
2003 |
Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.800 |
GeneticVariation
|
disease |
UNIPROT |
Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy.
|
12821740 |
2003 |
Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.800 |
CausalMutation
|
disease |
CLINVAR |
Mutations of sodium channel alpha subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures.
|
12566275 |
2003 |
Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.800 |
GeneticVariation
|
disease |
UNIPROT |
Sodium channel alpha1-subunit mutations in severe myoclonic epilepsy of infancy and infantile spasms.
|
14504318 |
2003 |
SCN1A-AS1
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
Mutations of sodium channel alpha subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures.
|
12566275 |
2003 |
SCN1A-AS1
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy.
|
12754708 |
2003 |
SCN1A-AS1
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy.
|
12821740 |
2003 |
Entrez Id: |
6323 |
Gene Symbol: |
SCN1A |
SCN1A
|
0.800 |
GeneticVariation
|
disease |
UNIPROT |
Clinical correlations of mutations in the SCN1A gene: from febrile seizures to severe myoclonic epilepsy in infancy.
|
15087100 |
2004 |