|
| Entrez Id: |
477 |
| Gene Symbol: |
ATP1A2 |
ATP1A2
|
Movement Disorders
|
0.100 |
CausalMutation |
CLINVAR |
Diagnostic Targeted Resequencing in 349 Patients with Drug-Resistant Pediatric Epilepsies Identifies Causative Mutations in 30 Different Genes.
|
27864847 |
2017 |
|
| Entrez Id: |
477 |
| Gene Symbol: |
ATP1A2 |
ATP1A2
|
Movement Disorders
|
0.100 |
CausalMutation |
CLINVAR |
An Infant With Epilepsy and Recurrent Hemiplegia due to Compound Heterozygous Variants in ATP1A2.
|
28811059 |
2017 |
|
| Entrez Id: |
477 |
| Gene Symbol: |
ATP1A2 |
ATP1A2
|
Movement Disorders
|
0.100 |
CausalMutation |
CLINVAR |
A missense variant of the ATP1A2 gene is associated with a novel phenotype of progressive sensorineural hearing loss associated with migraine.
|
25138102 |
2015 |
|
| Entrez Id: |
477 |
| Gene Symbol: |
ATP1A2 |
ATP1A2
|
Movement Disorders
|
0.100 |
CausalMutation |
CLINVAR |
A novel ATP1A2 gene mutation in familial hemiplegic migraine and epilepsy.
|
23918834 |
2014 |
|
| Entrez Id: |
477 |
| Gene Symbol: |
ATP1A2 |
ATP1A2
|
Movement Disorders
|
0.100 |
CausalMutation |
CLINVAR |
De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine.
|
20837964 |
2010 |
|
| Entrez Id: |
477 |
| Gene Symbol: |
ATP1A2 |
ATP1A2
|
Movement Disorders
|
0.100 |
CausalMutation |
CLINVAR |
First case of compound heterozygosity in Na,K-ATPase gene ATP1A2 in familial hemiplegic migraine.
|
17473835 |
2007 |
|
| Entrez Id: |
477 |
| Gene Symbol: |
ATP1A2 |
ATP1A2
|
Movement Disorders
|
0.100 |
CausalMutation |
CLINVAR |
ATP1A2 mutations in 11 families with familial hemiplegic migraine.
|
16088919 |
2005 |
|
| Entrez Id: |
477 |
| Gene Symbol: |
ATP1A2 |
ATP1A2
|
Movement Disorders
|
0.100 |
CausalMutation |
CLINVAR |
Familial basilar migraine associated with a new mutation in the ATP1A2 gene.
|
16344534 |
2005 |
|
| Entrez Id: |
477 |
| Gene Symbol: |
ATP1A2 |
ATP1A2
|
Movement Disorders
|
0.100 |
CausalMutation |
CLINVAR |
A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhood.
|
15286158 |
2004 |
|
| Entrez Id: |
477 |
| Gene Symbol: |
ATP1A2 |
ATP1A2
|
Movement Disorders
|
0.100 |
CausalMutation |
CLINVAR |
Alternating hemiplegia of childhood or familial hemiplegic migraine? A novel ATP1A2 mutation.
|
15174025 |
2004 |
|
| Entrez Id: |
477 |
| Gene Symbol: |
ATP1A2 |
ATP1A2
|
Movement Disorders
|
0.100 |
CausalMutation |
CLINVAR |
Alternating hemiplegia of childhood: a syndrome inherited with an autosomal dominant trait.
|
14667076 |
2003 |
|
| Entrez Id: |
477 |
| Gene Symbol: |
ATP1A2 |
ATP1A2
|
Movement Disorders
|
0.100 |
CausalMutation |
CLINVAR |
A syndrome of autosomal dominant alternating hemiplegia: clinical presentation mimicking intractable epilepsy; chromosomal studies; and physiologic investigations.
|
1361034 |
1992 |