×
Entrez Id:
111
Gene Symbol:
ADCY5
ADCY5
Movement Disorders
0.170
GeneticVariation
CLINVAR
ADCY5-related movement disorders: Frequency, disease course and phenotypic variability in a cohort of paediatric patients.
28511835
2017
×
Entrez Id:
111
Gene Symbol:
ADCY5
ADCY5
Movement Disorders
0.170
CausalMutation
CLINVAR
ADCY5-related dyskinesia presenting as familial myoclonus-dystonia.
28229249
2017
×
Entrez Id:
111
Gene Symbol:
ADCY5
ADCY5
Movement Disorders
0.170
CausalMutation
CLINVAR
ADCY5-related movement disorders: Frequency, disease course and phenotypic variability in a cohort of paediatric patients.
28511835
2017
×
Entrez Id:
111
Gene Symbol:
ADCY5
ADCY5
Movement Disorders
0.170
GeneticVariation
CLINVAR
ADCY5-related dyskinesia presenting as familial myoclonus-dystonia.
28229249
2017
×
Entrez Id:
111
Gene Symbol:
ADCY5
ADCY5
Movement Disorders
0.170
CausalMutation
CLINVAR
Treatment of ADCY5-Associated Dystonia, Chorea, and Hyperkinetic Disorders With Deep Brain Stimulation: A Multicenter Case Series.
27052971
2016
×
Entrez Id:
111
Gene Symbol:
ADCY5
ADCY5
Movement Disorders
0.170
GeneticVariation
CLINVAR
Treatment of ADCY5-Associated Dystonia, Chorea, and Hyperkinetic Disorders With Deep Brain Stimulation: A Multicenter Case Series.
27052971
2016
×
Entrez Id:
111
Gene Symbol:
ADCY5
ADCY5
Movement Disorders
0.170
GeneticVariation
CLINVAR
ADCY5 mutation carriers display pleiotropic paroxysmal day and nighttime dyskinesias.
26686870
2016
×
Entrez Id:
111
Gene Symbol:
ADCY5
ADCY5
Movement Disorders
0.170
GeneticVariation
CLINVAR
Phenotypic insights into ADCY5-associated disease.
27061943
2016
×
Entrez Id:
111
Gene Symbol:
ADCY5
ADCY5
Movement Disorders
0.170
CausalMutation
CLINVAR
Phenotypic insights into ADCY5-associated disease.
27061943
2016
×
Entrez Id:
111
Gene Symbol:
ADCY5
ADCY5
Movement Disorders
0.170
CausalMutation
CLINVAR
ADCY5 mutation carriers display pleiotropic paroxysmal day and nighttime dyskinesias.
26686870
2016
×
Entrez Id:
111
Gene Symbol:
ADCY5
ADCY5
Movement Disorders
0.170
GeneticVariation
CLINVAR
ADCY5 mutations are another cause of benign hereditary chorea.
26085604
2015
×
Entrez Id:
111
Gene Symbol:
ADCY5
ADCY5
Movement Disorders
0.170
CausalMutation
CLINVAR
ADCY5 mutations are another cause of benign hereditary chorea.
26085604
2015
×
Entrez Id:
111
Gene Symbol:
ADCY5
ADCY5
Movement Disorders
0.170
GeneticVariation
CLINVAR
ADCY5-related dyskinesia: Broader spectrum and genotype-phenotype correlations.
26537056
2015
×
Entrez Id:
111
Gene Symbol:
ADCY5
ADCY5
Movement Disorders
0.170
GeneticVariation
CLINVAR
A genome sequencing program for novel undiagnosed diseases.
25790160
2015
×
Entrez Id:
111
Gene Symbol:
ADCY5
ADCY5
Movement Disorders
0.170
CausalMutation
CLINVAR
ADCY5-related dyskinesia: Broader spectrum and genotype-phenotype correlations.
26537056
2015
×
Entrez Id:
111
Gene Symbol:
ADCY5
ADCY5
Movement Disorders
0.170
CausalMutation
CLINVAR
A genome sequencing program for novel undiagnosed diseases.
25790160
2015
×
Entrez Id:
111
Gene Symbol:
ADCY5
ADCY5
Movement Disorders
0.170
CausalMutation
CLINVAR
4-Phenylbutyrate attenuates the ER stress response and cyclic AMP accumulation in DYT1 dystonia cell models.
25379658
2014
×
Entrez Id:
111
Gene Symbol:
ADCY5
ADCY5
Movement Disorders
0.170
CausalMutation
CLINVAR
Gain-of-function ADCY5 mutations in familial dyskinesia with facial myokymia.
24700542
2014
×
Entrez Id:
111
Gene Symbol:
ADCY5
ADCY5
Movement Disorders
0.170
GeneticVariation
CLINVAR
4-Phenylbutyrate attenuates the ER stress response and cyclic AMP accumulation in DYT1 dystonia cell models.
25379658
2014
×
Entrez Id:
111
Gene Symbol:
ADCY5
ADCY5
Movement Disorders
0.170
GeneticVariation
CLINVAR
Structure, mechanism, and regulation of soluble adenylyl cyclases - similarities and differences to transmembrane adenylyl cyclases.
25193033
2014
×
Entrez Id:
111
Gene Symbol:
ADCY5
ADCY5
Movement Disorders
0.170
GeneticVariation
CLINVAR
Gain-of-function ADCY5 mutations in familial dyskinesia with facial myokymia.
24700542
2014
×
Entrez Id:
111
Gene Symbol:
ADCY5
ADCY5
Movement Disorders
0.170
CausalMutation
CLINVAR
Structure, mechanism, and regulation of soluble adenylyl cyclases - similarities and differences to transmembrane adenylyl cyclases.
25193033
2014
×
Entrez Id:
111
Gene Symbol:
ADCY5
ADCY5
Movement Disorders
0.170
GeneticVariation
CLINVAR
Role of Gα(olf) in familial and sporadic adult-onset primary dystonia.
23449625
2013
×
Entrez Id:
111
Gene Symbol:
ADCY5
ADCY5
Movement Disorders
0.170
CausalMutation
CLINVAR
Role of Gα(olf) in familial and sporadic adult-onset primary dystonia.
23449625
2013
×
Entrez Id:
111
Gene Symbol:
ADCY5
ADCY5
Movement Disorders
0.170
CausalMutation
CLINVAR
Gα(olf) mutation allows parsing the role of cAMP-dependent and extracellular signal-regulated kinase-dependent signaling in L-3,4-dihydroxyphenylalanine-induced dyskinesia.
22539851
2012