rs121908223
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Hemiplegic migraine, familial type 1
0.700
GeneticVariation
UNIPROT
Cerebellar Atrophy and Changes in Cytokines Associated with the CACNA1A R583Q Mutation in a Russian Familial Hemiplegic Migraine Type 1 Family.
28900389
2017
rs121908223
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Hemiplegic migraine, familial type 1
0.700
GeneticVariation
UNIPROT
A Single Amino Acid Deletion (ΔF1502) in the S6 Segment of CaV2.1 Domain III Associated with Congenital Ataxia Increases Channel Activity and Promotes Ca2+ Influx.
26716990
2015
rs121908223
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Hemiplegic migraine, familial type 1
0.700
GeneticVariation
UNIPROT
Congenital ataxia and hemiplegic migraine with cerebral edema associated with a novel gain of function mutation in the calcium channel CACNA1A.
24836863
2014
rs121908223
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Hemiplegic migraine, familial type 1
0.700
GeneticVariation
UNIPROT
EFNS guidelines on the molecular diagnosis of channelopathies, epilepsies, migraine, stroke, and dementias.
20298421
2010
rs121908223
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Hemiplegic migraine, familial type 1
0.700
GeneticVariation
UNIPROT
CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraine.
18400034
2008
rs121908223
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Hemiplegic migraine, familial type 1
0.700
GeneticVariation
UNIPROT
A novel R1347Q mutation in the predicted voltage sensor segment of the P/Q-type calcium-channel alpha-subunit in a family with progressive cerebellar ataxia and hemiplegic migraine.
15032980
2004
rs121908223
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Hemiplegic migraine, familial type 1
0.700
GeneticVariation
UNIPROT
Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine.
11409427
2001
rs121908223
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Hemiplegic migraine, familial type 1
0.700
GeneticVariation
UNIPROT
The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.
11439943
2001
rs121908223
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Hemiplegic migraine, familial type 1
0.700
GeneticVariation
UNIPROT
Genetic heterogeneity in Italian families with familial hemiplegic migraine.
10408532
1999
rs121908223
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Hemiplegic migraine, familial type 1
0.700
GeneticVariation
UNIPROT
Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.
8898206
1996