rs1553732126
|
|
CG |
0.700 |
GeneticVariation |
CLINVAR |
ADCY5-related movement disorders: Frequency, disease course and phenotypic variability in a cohort of paediatric patients.
|
28511835 |
2017 |
rs1553732126
|
|
CG |
0.700 |
GeneticVariation |
CLINVAR |
ADCY5-related dyskinesia presenting as familial myoclonus-dystonia.
|
28229249 |
2017 |
rs746547282
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
ADCY5-related dyskinesia presenting as familial myoclonus-dystonia.
|
28229249 |
2017 |
rs746547282
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
ADCY5-related movement disorders: Frequency, disease course and phenotypic variability in a cohort of paediatric patients.
|
28511835 |
2017 |
rs1553732126
|
|
CG |
0.700 |
GeneticVariation |
CLINVAR |
Treatment of ADCY5-Associated Dystonia, Chorea, and Hyperkinetic Disorders With Deep Brain Stimulation: A Multicenter Case Series.
|
27052971 |
2016 |
rs1553732126
|
|
CG |
0.700 |
GeneticVariation |
CLINVAR |
Phenotypic insights into ADCY5-associated disease.
|
27061943 |
2016 |
rs1553732126
|
|
CG |
0.700 |
GeneticVariation |
CLINVAR |
ADCY5 mutation carriers display pleiotropic paroxysmal day and nighttime dyskinesias.
|
26686870 |
2016 |
rs746547282
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Phenotypic insights into ADCY5-associated disease.
|
27061943 |
2016 |
rs746547282
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
ADCY5 mutation carriers display pleiotropic paroxysmal day and nighttime dyskinesias.
|
26686870 |
2016 |
rs746547282
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Treatment of ADCY5-Associated Dystonia, Chorea, and Hyperkinetic Disorders With Deep Brain Stimulation: A Multicenter Case Series.
|
27052971 |
2016 |
rs1553732126
|
|
CG |
0.700 |
GeneticVariation |
CLINVAR |
ADCY5-related dyskinesia: Broader spectrum and genotype-phenotype correlations.
|
26537056 |
2015 |
rs1553732126
|
|
CG |
0.700 |
GeneticVariation |
CLINVAR |
ADCY5 mutations are another cause of benign hereditary chorea.
|
26085604 |
2015 |
rs1553732126
|
|
CG |
0.700 |
GeneticVariation |
CLINVAR |
A genome sequencing program for novel undiagnosed diseases.
|
25790160 |
2015 |
rs746547282
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
A genome sequencing program for novel undiagnosed diseases.
|
25790160 |
2015 |
rs746547282
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
ADCY5-related dyskinesia: Broader spectrum and genotype-phenotype correlations.
|
26537056 |
2015 |
rs746547282
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
ADCY5 mutations are another cause of benign hereditary chorea.
|
26085604 |
2015 |
rs1553732126
|
|
CG |
0.700 |
GeneticVariation |
CLINVAR |
4-Phenylbutyrate attenuates the ER stress response and cyclic AMP accumulation in DYT1 dystonia cell models.
|
25379658 |
2014 |
rs1553732126
|
|
CG |
0.700 |
GeneticVariation |
CLINVAR |
Structure, mechanism, and regulation of soluble adenylyl cyclases - similarities and differences to transmembrane adenylyl cyclases.
|
25193033 |
2014 |
rs1553732126
|
|
CG |
0.700 |
GeneticVariation |
CLINVAR |
Gain-of-function ADCY5 mutations in familial dyskinesia with facial myokymia.
|
24700542 |
2014 |
rs746547282
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Gain-of-function ADCY5 mutations in familial dyskinesia with facial myokymia.
|
24700542 |
2014 |
rs746547282
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Structure, mechanism, and regulation of soluble adenylyl cyclases - similarities and differences to transmembrane adenylyl cyclases.
|
25193033 |
2014 |
rs746547282
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
4-Phenylbutyrate attenuates the ER stress response and cyclic AMP accumulation in DYT1 dystonia cell models.
|
25379658 |
2014 |
rs1553732126
|
|
CG |
0.700 |
GeneticVariation |
CLINVAR |
Role of Gα(olf) in familial and sporadic adult-onset primary dystonia.
|
23449625 |
2013 |
rs746547282
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Role of Gα(olf) in familial and sporadic adult-onset primary dystonia.
|
23449625 |
2013 |
rs1553732126
|
|
CG |
0.700 |
GeneticVariation |
CLINVAR |
Autosomal dominant familial dyskinesia and facial myokymia: single exome sequencing identifies a mutation in adenylyl cyclase 5.
|
22782511 |
2012 |