rs1554767313
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
DNM1 encephalopathy: A new disease of vesicle fission.
|
28667181 |
2017 |
rs1554767317
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
DNM1 encephalopathy: A new disease of vesicle fission.
|
28667181 |
2017 |
rs1554767313
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
De novo DNM1 mutations in two cases of epileptic encephalopathy.
|
26611353 |
2016 |
rs1554767313
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Unexplained early onset epileptic encephalopathy: Exome screening and phenotype expansion.
|
26648591 |
2016 |
rs1554767317
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
De novo DNM1 mutations in two cases of epileptic encephalopathy.
|
26611353 |
2016 |
rs1554767317
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Unexplained early onset epileptic encephalopathy: Exome screening and phenotype expansion.
|
26648591 |
2016 |
rs1554767313
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Large-scale discovery of novel genetic causes of developmental disorders.
|
25533962 |
2015 |
rs1554767317
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Large-scale discovery of novel genetic causes of developmental disorders.
|
25533962 |
2015 |
rs1554767313
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
De novo mutations in synaptic transmission genes including DNM1 cause epileptic encephalopathies.
|
25262651 |
2014 |
rs1554767317
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
De novo mutations in synaptic transmission genes including DNM1 cause epileptic encephalopathies.
|
25262651 |
2014 |
rs1554767313
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Dynamin 2 homozygous mutation in humans with a lethal congenital syndrome.
|
23092955 |
2013 |
rs1554767313
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Building a fission machine--structural insights into dynamin assembly and activation.
|
23781021 |
2013 |
rs1554767317
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Building a fission machine--structural insights into dynamin assembly and activation.
|
23781021 |
2013 |
rs1554767317
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Dynamin 2 homozygous mutation in humans with a lethal congenital syndrome.
|
23092955 |
2013 |
rs1554767313
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Dynamin, a membrane-remodelling GTPase.
|
22233676 |
2012 |
rs1554767317
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Dynamin, a membrane-remodelling GTPase.
|
22233676 |
2012 |
rs1554767313
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Recruitment of endophilin to clathrin-coated pit necks is required for efficient vesicle uncoating after fission.
|
22099461 |
2011 |
rs1554767313
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Proper synaptic vesicle formation and neuronal network activity critically rely on syndapin I.
|
21926968 |
2011 |
rs1554767313
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function.
|
21441247 |
2011 |
rs1554767313
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
The crystal structure of dynamin.
|
21927001 |
2011 |
rs1554767317
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
The crystal structure of dynamin.
|
21927001 |
2011 |
rs1554767317
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function.
|
21441247 |
2011 |
rs1554767317
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Proper synaptic vesicle formation and neuronal network activity critically rely on syndapin I.
|
21926968 |
2011 |
rs1554767317
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Recruitment of endophilin to clathrin-coated pit necks is required for efficient vesicle uncoating after fission.
|
22099461 |
2011 |
rs1554767313
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
G domain dimerization controls dynamin's assembly-stimulated GTPase activity.
|
20428113 |
2010 |