Migraine, Familial Hemiplegic, 3
|
0.700 |
Biomarker
|
disease |
CTD_human |
|
|
|
Migraine, Familial Hemiplegic, 3
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
|
|
|
Migraine, Familial Hemiplegic, 3
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
|
|
|
Migraine, Familial Hemiplegic, 3
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
|
|
|
Migraine, Familial Hemiplegic, 3
|
0.700 |
Biomarker
|
disease |
CLINGEN |
A novel SCN1A mutation identified in a Chinese family with familial hemiplegic migraine: A case report.
|
27919014 |
2017 |
Migraine, Familial Hemiplegic, 3
|
0.700 |
Biomarker
|
disease |
CLINGEN |
Clinical and electroencephalographic abnormalities during the full duration of a sporadic hemiplegic migraine attack.
|
27155821 |
2016 |
Migraine, Familial Hemiplegic, 3
|
0.700 |
Biomarker
|
disease |
CLINGEN |
Early-onset familial hemiplegic migraine due to a novel SCN1A mutation.
|
26763045 |
2016 |
Migraine, Familial Hemiplegic, 3
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations.
|
19332696 |
2009 |
Migraine, Familial Hemiplegic, 3
|
0.700 |
Biomarker
|
disease |
CLINGEN |
Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations.
|
19332696 |
2009 |
Migraine, Familial Hemiplegic, 3
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations.
|
19332696 |
2009 |
Migraine, Familial Hemiplegic, 3
|
0.700 |
Biomarker
|
disease |
CLINGEN |
Familial hemiplegic migraine due to L263V SCN1A mutation: discordance for epilepsy between two kindreds from Douro Valley.
|
24646837 |
2014 |
Migraine, Familial Hemiplegic, 3
|
0.700 |
Biomarker
|
disease |
CLINGEN |
Familial Hemiplegic Migraine Type 3 (FHM3) With an SCN1A Mutation in a Chinese Family: A Case Report.
|
30498473 |
2018 |
Migraine, Familial Hemiplegic, 3
|
0.700 |
Biomarker
|
disease |
CLINGEN |
First mutation in the voltage-gated Nav1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsy.
|
19220312 |
2009 |
Migraine, Familial Hemiplegic, 3
|
0.700 |
Biomarker
|
disease |
CLINGEN |
Gain of Function for the SCN1A/hNav1.1-L1670W Mutation Responsible for Familial Hemiplegic Migraine.
|
30038559 |
2018 |
Migraine, Familial Hemiplegic, 3
|
0.700 |
Biomarker
|
disease |
CLINGEN |
Genetic studies of Polish migraine patients: screening for causative mutations in four migraine-associated genes.
|
26747084 |
2016 |
Migraine, Familial Hemiplegic, 3
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine.
|
16054936 |
2005 |
Migraine, Familial Hemiplegic, 3
|
0.700 |
Biomarker
|
disease |
CLINGEN |
Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine.
|
16054936 |
2005 |
Migraine, Familial Hemiplegic, 3
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2.
|
10742094 |
2000 |
Migraine, Familial Hemiplegic, 3
|
0.700 |
Biomarker
|
disease |
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 |
Migraine, Familial Hemiplegic, 3
|
0.700 |
Biomarker
|
disease |
CLINGEN |
Novel mutation confirms seizure locus SCN1A is also familial hemiplegic migraine locus FHM3.
|
18021921 |
2007 |
Migraine, Familial Hemiplegic, 3
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
Novel mutation confirms seizure locus SCN1A is also familial hemiplegic migraine locus FHM3.
|
18021921 |
2007 |
Migraine, Familial Hemiplegic, 3
|
0.700 |
Biomarker
|
disease |
CLINGEN |
Self-limited hyperexcitability: functional effect of a familial hemiplegic migraine mutation of the Nav1.1 (SCN1A) Na+ channel.
|
18632931 |
2008 |
Migraine, Familial Hemiplegic, 3
|
0.700 |
Biomarker
|
disease |
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 |
Migraine, Familial Hemiplegic, 3
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
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 |
Migraine, Familial Hemiplegic, 3
|
0.700 |
Biomarker
|
disease |
CLINGEN |
Two novel families with hemiplegic migraine caused by recurrent SCN1A mutation p.F1499L.
|
29145747 |
2018 |