rs121908213
|
|
|
0.820 |
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 |
rs121908213
|
|
G |
0.820 |
CausalMutation |
CLINVAR |
|
|
|
rs121908213
|
|
|
0.820 |
GeneticVariation |
UNIPROT |
Genetic heterogeneity in Italian families with familial hemiplegic migraine.
|
10408532 |
1999 |
rs121908213
|
|
|
0.820 |
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 |
rs121908213
|
|
|
0.820 |
GeneticVariation |
UNIPROT |
Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.
|
8898206 |
1996 |
rs121908213
|
|
|
0.820 |
GeneticVariation |
UNIPROT |
CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraine.
|
18400034 |
2008 |
rs121908213
|
|
|
0.820 |
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 |
rs121908213
|
|
|
0.820 |
GeneticVariation |
BEFREE |
We analyzed the phenotype-genotype relation in three unrelated FHM families with the calcium channel alpha1A-subunit gene mutations I1811L (two families) and V714A (one family).
|
9566402 |
1998 |
rs121908213
|
|
|
0.820 |
GeneticVariation |
UNIPROT |
The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.
|
11439943 |
2001 |
rs121908213
|
|
|
0.820 |
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 |
rs121908213
|
|
|
0.820 |
GeneticVariation |
BEFREE |
To obtain data from direct gene analysis to test this hypothesis, we investigated 143 patients with common migraine, irrespective of their family history, for the presence of mutations known to result in the FHM phenotype; the mutations V714A, R192Q, R583Q, T666M, V1457L, and 11811L were absent in our patient sample.
|
12705332 |
2003 |
rs121908213
|
|
|
0.820 |
GeneticVariation |
UNIPROT |
EFNS guidelines on the molecular diagnosis of channelopathies, epilepsies, migraine, stroke, and dementias.
|
20298421 |
2010 |
rs121908213
|
|
|
0.820 |
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 |