×
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