rs1555951954
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Alu-specific microhomology-mediated deletions in CDKL5 in females with early-onset seizure disorder.
|
19471977 |
2009 |
rs786204963
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Alu-specific microhomology-mediated deletions in CDKL5 in females with early-onset seizure disorder.
|
19471977 |
2009 |
rs786204967
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Alu-specific microhomology-mediated deletions in CDKL5 in females with early-onset seizure disorder.
|
19471977 |
2009 |
rs1555951954
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
CDKL5 and ARX mutations in males with early-onset epilepsy.
|
23583054 |
2013 |
rs786204963
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
CDKL5 and ARX mutations in males with early-onset epilepsy.
|
23583054 |
2013 |
rs786204967
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
CDKL5 and ARX mutations in males with early-onset epilepsy.
|
23583054 |
2013 |
rs1555951954
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
CDKL5-Related Disorders: From Clinical Description to Molecular Genetics.
|
22670135 |
2012 |
rs786204963
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
CDKL5-Related Disorders: From Clinical Description to Molecular Genetics.
|
22670135 |
2012 |
rs786204967
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
CDKL5-Related Disorders: From Clinical Description to Molecular Genetics.
|
22670135 |
2012 |
rs1555951954
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Clinical features and gene mutational spectrum of CDKL5-related diseases in a cohort of Chinese patients.
|
24564546 |
2014 |
rs786204963
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Clinical features and gene mutational spectrum of CDKL5-related diseases in a cohort of Chinese patients.
|
24564546 |
2014 |
rs786204967
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Clinical features and gene mutational spectrum of CDKL5-related diseases in a cohort of Chinese patients.
|
24564546 |
2014 |
rs1555951954
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Functional abilities in children and adults with the CDKL5 disorder.
|
27528505 |
2016 |
rs786204963
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Functional abilities in children and adults with the CDKL5 disorder.
|
27528505 |
2016 |
rs786204967
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Functional abilities in children and adults with the CDKL5 disorder.
|
27528505 |
2016 |
rs1555951954
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
GluD1 is a common altered player in neuronal differentiation from both MECP2-mutated and CDKL5-mutated iPS cells.
|
24916645 |
2015 |
rs786204963
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
GluD1 is a common altered player in neuronal differentiation from both MECP2-mutated and CDKL5-mutated iPS cells.
|
24916645 |
2015 |
rs786204967
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
GluD1 is a common altered player in neuronal differentiation from both MECP2-mutated and CDKL5-mutated iPS cells.
|
24916645 |
2015 |
rs1555951954
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Mutation screening of the CDKL5 gene in cryptogenic infantile intractable epilepsy and review of clinical sensitivity.
|
21775177 |
2011 |
rs786204963
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Mutation screening of the CDKL5 gene in cryptogenic infantile intractable epilepsy and review of clinical sensitivity.
|
21775177 |
2011 |
rs786204967
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Mutation screening of the CDKL5 gene in cryptogenic infantile intractable epilepsy and review of clinical sensitivity.
|
21775177 |
2011 |
rs1555951954
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Mutational spectrum of CDKL5 in early-onset encephalopathies: a study of a large collection of French patients and review of the literature.
|
19793311 |
2009 |
rs786204963
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Mutational spectrum of CDKL5 in early-onset encephalopathies: a study of a large collection of French patients and review of the literature.
|
19793311 |
2009 |
rs786204967
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Mutational spectrum of CDKL5 in early-onset encephalopathies: a study of a large collection of French patients and review of the literature.
|
19793311 |
2009 |
rs1555951954
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Mutations in UNC80, Encoding Part of the UNC79-UNC80-NALCN Channel Complex, Cause Autosomal-Recessive Severe Infantile Encephalopathy.
|
26708753 |
2016 |