×
Entrez Id:
6323
Gene Symbol:
SCN1A
SCN1A
Migraine, Familial Hemiplegic, 3
0.700
Biomarker
CLINGEN
Two novel families with hemiplegic migraine caused by recurrent SCN1A mutation p.F1499L.
29145747
2018
×
Entrez Id:
6323
Gene Symbol:
SCN1A
SCN1A
Migraine, Familial Hemiplegic, 3
0.700
Biomarker
CLINGEN
Familial Hemiplegic Migraine Type 3 (FHM3) With an SCN1A Mutation in a Chinese Family: A Case Report.
30498473
2018
×
Entrez Id:
6323
Gene Symbol:
SCN1A
SCN1A
Migraine, Familial Hemiplegic, 3
0.700
Biomarker
CLINGEN
Gain of Function for the SCN1A /hNav 1.1-L1670W Mutation Responsible for Familial Hemiplegic Migraine.
30038559
2018
×
Entrez Id:
6323
Gene Symbol:
SCN1A
SCN1A
Migraine, Familial Hemiplegic, 3
0.700
Biomarker
CLINGEN
A novel SCN1A mutation identified in a Chinese family with familial hemiplegic migraine: A case report.
27919014
2017
×
Entrez Id:
6323
Gene Symbol:
SCN1A
SCN1A
Migraine, Familial Hemiplegic, 3
0.700
Biomarker
CLINGEN
Early-onset familial hemiplegic migraine due to a novel SCN1A mutation.
26763045
2016
×
Entrez Id:
6323
Gene Symbol:
SCN1A
SCN1A
Migraine, Familial Hemiplegic, 3
0.700
Biomarker
CLINGEN
Clinical and electroencephalographic abnormalities during the full duration of a sporadic hemiplegic migraine attack.
27155821
2016
×
Entrez Id:
6323
Gene Symbol:
SCN1A
SCN1A
Migraine, Familial Hemiplegic, 3
0.700
Biomarker
CLINGEN
Genetic studies of Polish migraine patients: screening for causative mutations in four migraine-associated genes.
26747084
2016
×
Entrez Id:
6323
Gene Symbol:
SCN1A
SCN1A
Migraine, Familial Hemiplegic, 3
0.700
Biomarker
CLINGEN
Familial hemiplegic migraine due to L263V SCN1A mutation: discordance for epilepsy between two kindreds from Douro Valley.
24646837
2014
×
Entrez Id:
6323
Gene Symbol:
SCN1A
SCN1A
Migraine, Familial Hemiplegic, 3
0.700
Biomarker
CLINGEN
Two novel SCN1A mutations identified in families with familial hemiplegic migraine.
24707016
2014
×
Entrez Id:
6323
Gene Symbol:
SCN1A
SCN1A
Migraine, Familial Hemiplegic, 3
0.700
Biomarker
CLINGEN
First mutation in the voltage-gated Nav1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsy.
19220312
2009
×
Entrez Id:
6323
Gene Symbol:
SCN1A
SCN1A
Migraine, Familial Hemiplegic, 3
0.700
Biomarker
CLINGEN
Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations.
19332696
2009
×
Entrez Id:
6323
Gene Symbol:
SCN1A
SCN1A
Migraine, Familial Hemiplegic, 3
0.700
Biomarker
CLINGEN
Self-limited hyperexcitability: functional effect of a familial hemiplegic migraine mutation of the Nav1.1 (SCN1A) Na+ channel.
18632931
2008
×
Entrez Id:
6323
Gene Symbol:
SCN1A
SCN1A
Migraine, Familial Hemiplegic, 3
0.700
Biomarker
CLINGEN
Novel mutation confirms seizure locus SCN1A is also familial hemiplegic migraine locus FHM3.
18021921
2007
×
Entrez Id:
6323
Gene Symbol:
SCN1A
SCN1A
Migraine, Familial Hemiplegic, 3
0.700
Biomarker
CLINGEN
The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. Online.
17397047
2007
×
Entrez Id:
6323
Gene Symbol:
SCN1A
SCN1A
Migraine, Familial Hemiplegic, 3
0.700
Biomarker
CLINGEN
Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation.
17537961
2007
×
Entrez Id:
6323
Gene Symbol:
SCN1A
SCN1A
Migraine, Familial Hemiplegic, 3
0.700
Biomarker
CLINGEN
Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine.
16054936
2005