×
Entrez Id:
478
Gene Symbol:
ATP1A3
ATP1A3
Muscle hypotonia
0.100
CausalMutation
CLINVAR
Chromosomal localization of human Na+, K+-ATPase alpha- and beta-subunit genes.
2842249
1988
×
Entrez Id:
478
Gene Symbol:
ATP1A3
ATP1A3
Muscle hypotonia
0.100
GeneticVariation
CLINVAR
Chromosomal localization of human Na+, K+-ATPase alpha- and beta-subunit genes.
2842249
1988
×
Entrez Id:
478
Gene Symbol:
ATP1A3
ATP1A3
Muscle hypotonia
0.100
GeneticVariation
CLINVAR
Alternating hemiplegia of childhood.
8496742
1993
×
Entrez Id:
478
Gene Symbol:
ATP1A3
ATP1A3
Muscle hypotonia
0.100
CausalMutation
CLINVAR
Alternating hemiplegia of childhood.
8496742
1993
×
Entrez Id:
478
Gene Symbol:
ATP1A3
ATP1A3
Muscle hypotonia
0.100
GeneticVariation
CLINVAR
Alternating hemiplegia of childhood: clinical manifestations and long-term outcome.
11020638
2000
×
Entrez Id:
478
Gene Symbol:
ATP1A3
ATP1A3
Muscle hypotonia
0.100
CausalMutation
CLINVAR
Alternating hemiplegia of childhood: clinical manifestations and long-term outcome.
11020638
2000
×
Entrez Id:
478
Gene Symbol:
ATP1A3
ATP1A3
Muscle hypotonia
0.100
CausalMutation
CLINVAR
Mutations in the Na+/K+ -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism.
15260953
2004
×
Entrez Id:
478
Gene Symbol:
ATP1A3
ATP1A3
Muscle hypotonia
0.100
GeneticVariation
CLINVAR
Mutations in the Na+/K+ -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism.
15260953
2004
×
Entrez Id:
478
Gene Symbol:
ATP1A3
ATP1A3
Muscle hypotonia
0.100
GeneticVariation
CLINVAR
Mutations Phe785Leu and Thr618Met in Na+,K+-ATPase, associated with familial rapid-onset dystonia parkinsonism, interfere with Na+ interaction by distinct mechanisms.
16632466
2006
×
Entrez Id:
478
Gene Symbol:
ATP1A3
ATP1A3
Muscle hypotonia
0.100
CausalMutation
CLINVAR
Mutations Phe785Leu and Thr618Met in Na+,K+-ATPase, associated with familial rapid-onset dystonia parkinsonism, interfere with Na+ interaction by distinct mechanisms.
16632466
2006
×
Entrez Id:
478
Gene Symbol:
ATP1A3
ATP1A3
Muscle hypotonia
0.100
CausalMutation
CLINVAR
Rapid-onset dystonia-parkinsonism in a child with a novel atp1a3 gene mutation.
19652145
2009
×
Entrez Id:
478
Gene Symbol:
ATP1A3
ATP1A3
Muscle hypotonia
0.100
GeneticVariation
CLINVAR
Rapid-onset dystonia-parkinsonism in a child with a novel atp1a3 gene mutation.
19652145
2009
×
Entrez Id:
478
Gene Symbol:
ATP1A3
ATP1A3
Muscle hypotonia
0.100
GeneticVariation
CLINVAR
New triggers and non-motor findings in a family with rapid-onset dystonia-parkinsonism.
22534615
2012
×
Entrez Id:
478
Gene Symbol:
ATP1A3
ATP1A3
Muscle hypotonia
0.100
GeneticVariation
CLINVAR
Psychiatric disorders in rapid-onset dystonia-parkinsonism.
22933743
2012
×
Entrez Id:
478
Gene Symbol:
ATP1A3
ATP1A3
Muscle hypotonia
0.100
CausalMutation
CLINVAR
Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study.
22850527
2012
×
Entrez Id:
478
Gene Symbol:
ATP1A3
ATP1A3
Muscle hypotonia
0.100
GeneticVariation
CLINVAR
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood.
22842232
2012
×
Entrez Id:
478
Gene Symbol:
ATP1A3
ATP1A3
Muscle hypotonia
0.100
CausalMutation
CLINVAR
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood.
22842232
2012
×
Entrez Id:
478
Gene Symbol:
ATP1A3
ATP1A3
Muscle hypotonia
0.100
GeneticVariation
CLINVAR
Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study.
22850527
2012
×
Entrez Id:
478
Gene Symbol:
ATP1A3
ATP1A3
Muscle hypotonia
0.100
GeneticVariation
CLINVAR
ATP1A3 mutations in infants: a new rapid-onset dystonia-Parkinsonism phenotype characterized by motor delay and ataxia.
22924536
2012
×
Entrez Id:
478
Gene Symbol:
ATP1A3
ATP1A3
Muscle hypotonia
0.100
CausalMutation
CLINVAR
New triggers and non-motor findings in a family with rapid-onset dystonia-parkinsonism.
22534615
2012
×
Entrez Id:
478
Gene Symbol:
ATP1A3
ATP1A3
Muscle hypotonia
0.100
CausalMutation
CLINVAR
ATP1A3 mutations in infants: a new rapid-onset dystonia-Parkinsonism phenotype characterized by motor delay and ataxia.
22924536
2012
×
Entrez Id:
478
Gene Symbol:
ATP1A3
ATP1A3
Muscle hypotonia
0.100
CausalMutation
CLINVAR
Psychiatric disorders in rapid-onset dystonia-parkinsonism.
22933743
2012
×
Entrez Id:
478
Gene Symbol:
ATP1A3
ATP1A3
Muscle hypotonia
0.100
CausalMutation
CLINVAR
The multiple faces of the ATP1A3-related dystonic movement disorder.
23483595
2013
×
Entrez Id:
478
Gene Symbol:
ATP1A3
ATP1A3
Muscle hypotonia
0.100
GeneticVariation
CLINVAR
The multiple faces of the ATP1A3-related dystonic movement disorder.
23483595
2013
×
Entrez Id:
478
Gene Symbol:
ATP1A3
ATP1A3
Muscle hypotonia
0.100
GeneticVariation
CLINVAR
Intermediate form between alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism.
24123283
2014