rs1318353774
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
De novo mutations in epileptic encephalopathies.
|
23934111 |
2013 |
rs1318353774
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
The International Classification of Headache Disorders, 3rd edition (beta version).
|
23771276 |
2013 |
rs1318353774
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Identification of a novel nonsense mutation p.Tyr1957Ter of CACNA1A in a Chinese family with episodic ataxia 2.
|
23441182 |
2013 |
rs1555756091
|
|
TA |
0.700 |
CausalMutation |
CLINVAR |
Identification of a novel nonsense mutation p.Tyr1957Ter of CACNA1A in a Chinese family with episodic ataxia 2.
|
23441182 |
2013 |
rs1555756091
|
|
TA |
0.700 |
CausalMutation |
CLINVAR |
The International Classification of Headache Disorders, 3rd edition (beta version).
|
23771276 |
2013 |
rs1555756091
|
|
TA |
0.700 |
CausalMutation |
CLINVAR |
Possible effect of corticoids on hemiplegic attacks in severe hemiplegic migraine.
|
23831250 |
2013 |
rs1555756091
|
|
TA |
0.700 |
CausalMutation |
CLINVAR |
De novo mutations in epileptic encephalopathies.
|
23934111 |
2013 |
rs886037945
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Possible effect of corticoids on hemiplegic attacks in severe hemiplegic migraine.
|
23831250 |
2013 |
rs886037945
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
De novo mutations in epileptic encephalopathies.
|
23934111 |
2013 |
rs886037945
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
The International Classification of Headache Disorders, 3rd edition (beta version).
|
23771276 |
2013 |
rs886037945
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Identification of a novel nonsense mutation p.Tyr1957Ter of CACNA1A in a Chinese family with episodic ataxia 2.
|
23441182 |
2013 |
rs1057520918
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Neuronal P/Q-type calcium channel dysfunction in inherited disorders of the CNS.
|
22249839 |
2012 |
rs1318353774
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Neuronal P/Q-type calcium channel dysfunction in inherited disorders of the CNS.
|
22249839 |
2012 |
rs1555756091
|
|
TA |
0.700 |
CausalMutation |
CLINVAR |
Neuronal P/Q-type calcium channel dysfunction in inherited disorders of the CNS.
|
22249839 |
2012 |
rs886037945
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Neuronal P/Q-type calcium channel dysfunction in inherited disorders of the CNS.
|
22249839 |
2012 |
rs1057520918
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Recurrent stroke due to a novel voltage sensor mutation in Cav2.1 responds to verapamil.
|
21183743 |
2011 |
rs1318353774
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Recurrent stroke due to a novel voltage sensor mutation in Cav2.1 responds to verapamil.
|
21183743 |
2011 |
rs1555756091
|
|
TA |
0.700 |
CausalMutation |
CLINVAR |
Recurrent stroke due to a novel voltage sensor mutation in Cav2.1 responds to verapamil.
|
21183743 |
2011 |
rs886037945
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Recurrent stroke due to a novel voltage sensor mutation in Cav2.1 responds to verapamil.
|
21183743 |
2011 |
rs1057520918
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Sporadic hemiplegic migraine and delayed cerebral oedema after minor head trauma: a novel de novo CACNA1A gene mutation.
|
19811514 |
2010 |
rs1057520918
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Genetic and functional characterisation of the P/Q calcium channel in episodic ataxia with epilepsy.
|
20156848 |
2010 |
rs1057520918
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Identification of novel and recurrent CACNA1A gene mutations in fifteen patients with episodic ataxia type 2.
|
20129625 |
2010 |
rs1057520918
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
CaV2.1 channelopathies.
|
20204399 |
2010 |
rs1057520918
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
A wide spectrum of clinical, neurophysiological and neuroradiological abnormalities in a family with a novel CACNA1A mutation.
|
20682717 |
2010 |
rs1057520918
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Congenital ataxia, mental retardation, and dyskinesia associated with a novel CACNA1A mutation.
|
20097664 |
2010 |