×
Entrez Id:
2775
Gene Symbol:
GNAO1
GNAO1
Movement Disorders
0.500
GeneticVariation
CLINVAR
×
Entrez Id:
23221
Gene Symbol:
RHOBTB2
RHOBTB2
Movement Disorders
0.110
GeneticVariation
CLINVAR
×
Entrez Id:
2629
Gene Symbol:
GBA
GBA
Movement Disorders
0.110
SusceptibilityMutation
CLINVAR
×
Entrez Id:
6857
Gene Symbol:
SYT1
SYT1
Movement Disorders
0.100
CausalMutation
CLINVAR
×
Entrez Id:
472
Gene Symbol:
ATM
ATM
Movement Disorders
0.100
GeneticVariation
CLINVAR
C11orf65
Movement Disorders
0.100
GeneticVariation
CLINVAR
×
Entrez Id:
5538
Gene Symbol:
PPT1
PPT1
Movement Disorders
0.100
CausalMutation
CLINVAR
×
Entrez Id:
253260
Gene Symbol:
RICTOR
RICTOR
Movement Disorders
0.100
GeneticVariation
CLINVAR
Nutrition education in the medical school curriculum: a proposal for action: a curriculum design.
2006
1976
×
Entrez Id:
1213
Gene Symbol:
CLTC
CLTC
Movement Disorders
0.100
GeneticVariation
CLINVAR
Clathrin: a unique protein associated with intracellular transfer of membrane by coated vesicles.
1063406
1976
×
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
×
Entrez Id:
2074
Gene Symbol:
ERCC6
ERCC6
Movement Disorders
0.100
CausalMutation
CLINVAR
Xeroderma pigmentosum and Cockayne syndrome: overlapping clinical and biochemical phenotypes.
1372469
1992
×
Entrez Id:
2893
Gene Symbol:
GRIA4
GRIA4
Movement Disorders
0.100
GeneticVariation
CLINVAR
Light and electron immunocytochemical localization of AMPA-selective glutamate receptors in the rat brain.
1374769
1992
×
Entrez Id:
3737
Gene Symbol:
KCNA2
KCNA2
Movement Disorders
0.100
CausalMutation
CLINVAR
An essential 'set' of K+ channels conserved in flies, mice and humans.
1377421
1992
×
Entrez Id:
3737
Gene Symbol:
KCNA2
KCNA2
Movement Disorders
0.100
GeneticVariation
CLINVAR
An essential 'set' of K+ channels conserved in flies, mice and humans.
1377421
1992
×
Entrez Id:
546
Gene Symbol:
ATRX
ATRX
Movement Disorders
0.100
CausalMutation
CLINVAR
X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome: localization to Xq12-q21.31 by X inactivation and linkage analysis.
1415255
1992
×
Entrez Id:
1788
Gene Symbol:
DNMT3A
DNMT3A
Movement Disorders
0.100
CausalMutation
CLINVAR
A targeting sequence directs DNA methyltransferase to sites of DNA replication in mammalian nuclei.
1423634
1992
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Movement Disorders
0.100
CausalMutation
CLINVAR
Familial paroxysmal ataxia: report of a family.
1564484
1992
×
Entrez Id:
111
Gene Symbol:
ADCY5
ADCY5
Movement Disorders
0.170
GeneticVariation
CLINVAR
Isolation and characterization of a novel cardiac adenylylcyclase cDNA.
1618857
1992
×
Entrez Id:
111
Gene Symbol:
ADCY5
ADCY5
Movement Disorders
0.170
CausalMutation
CLINVAR
Isolation and characterization of a novel cardiac adenylylcyclase cDNA.
1618857
1992
×
Entrez Id:
3737
Gene Symbol:
KCNA2
KCNA2
Movement Disorders
0.100
CausalMutation
CLINVAR
Determination of the subunit stoichiometry of a voltage-activated potassium channel.
1706481
1991
×
Entrez Id:
3737
Gene Symbol:
KCNA2
KCNA2
Movement Disorders
0.100
GeneticVariation
CLINVAR
Determination of the subunit stoichiometry of a voltage-activated potassium channel.
1706481
1991
×
Entrez Id:
5813
Gene Symbol:
PURA
PURA
Movement Disorders
0.100
CausalMutation
CLINVAR
Dendritic location of neural BC1 RNA.
1706516
1991
×
Entrez Id:
6513
Gene Symbol:
SLC2A1
SLC2A1
Movement Disorders
0.200
CausalMutation
CLINVAR
Defective glucose transport across the blood-brain barrier as a cause of persistent hypoglycorrhachia, seizures, and developmental delay.
1714544
1991
×
Entrez Id:
2902
Gene Symbol:
GRIN1
GRIN1
Movement Disorders
0.130
GeneticVariation
CLINVAR
Molecular cloning and characterization of the rat NMDA receptor.
1834949
1991
×
Entrez Id:
6651
Gene Symbol:
SON
SON
Movement Disorders
0.100
GeneticVariation
CLINVAR
[Identification of a protein product of a novel human gene SON and the biological effect upon administering a changed form of this gene into mammalian cells].
1944255
1991