rs773760466
|
Entrez Id: |
6792 |
Gene Symbol: |
CDKL5 |
CDKL5
|
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Clinical features and gene mutational spectrum of CDKL5-related diseases in a cohort of Chinese patients.
|
24564546 |
2014 |
rs866859766
|
RS1;CDKL5
|
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Clinical features and gene mutational spectrum of CDKL5-related diseases in a cohort of Chinese patients.
|
24564546 |
2014 |
rs267608468
|
Entrez Id: |
6792 |
Gene Symbol: |
CDKL5 |
CDKL5
|
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Targeted capture and sequencing for detection of mutations causing early onset epileptic encephalopathy.
|
23662938 |
2013 |
rs267608468
|
Entrez Id: |
6792 |
Gene Symbol: |
CDKL5 |
CDKL5
|
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.
|
23708187 |
2013 |
rs267608493
|
Entrez Id: |
6792 |
Gene Symbol: |
CDKL5 |
CDKL5
|
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.
|
23708187 |
2013 |
rs267608493
|
Entrez Id: |
6792 |
Gene Symbol: |
CDKL5 |
CDKL5
|
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Targeted capture and sequencing for detection of mutations causing early onset epileptic encephalopathy.
|
23662938 |
2013 |
rs267608501
|
Entrez Id: |
6792 |
Gene Symbol: |
CDKL5 |
CDKL5
|
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.
|
23708187 |
2013 |
rs267608501
|
Entrez Id: |
6792 |
Gene Symbol: |
CDKL5 |
CDKL5
|
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Targeted capture and sequencing for detection of mutations causing early onset epileptic encephalopathy.
|
23662938 |
2013 |
rs267608511
|
Entrez Id: |
6792 |
Gene Symbol: |
CDKL5 |
CDKL5
|
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Targeted capture and sequencing for detection of mutations causing early onset epileptic encephalopathy.
|
23662938 |
2013 |
rs267608511
|
Entrez Id: |
6792 |
Gene Symbol: |
CDKL5 |
CDKL5
|
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.
|
23708187 |
2013 |
rs267608611
|
Entrez Id: |
6792 |
Gene Symbol: |
CDKL5 |
CDKL5
|
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Targeted capture and sequencing for detection of mutations causing early onset epileptic encephalopathy.
|
23662938 |
2013 |
rs267608611
|
Entrez Id: |
6792 |
Gene Symbol: |
CDKL5 |
CDKL5
|
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.
|
23708187 |
2013 |
rs61749700
|
Entrez Id: |
6792 |
Gene Symbol: |
CDKL5 |
CDKL5
|
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Targeted capture and sequencing for detection of mutations causing early onset epileptic encephalopathy.
|
23662938 |
2013 |
rs61749700
|
Entrez Id: |
6792 |
Gene Symbol: |
CDKL5 |
CDKL5
|
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.
|
23708187 |
2013 |
rs61749704
|
Entrez Id: |
6792 |
Gene Symbol: |
CDKL5 |
CDKL5
|
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.
|
23708187 |
2013 |
rs61749704
|
Entrez Id: |
6792 |
Gene Symbol: |
CDKL5 |
CDKL5
|
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Targeted capture and sequencing for detection of mutations causing early onset epileptic encephalopathy.
|
23662938 |
2013 |
rs773760466
|
Entrez Id: |
6792 |
Gene Symbol: |
CDKL5 |
CDKL5
|
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.
|
23708187 |
2013 |
rs773760466
|
Entrez Id: |
6792 |
Gene Symbol: |
CDKL5 |
CDKL5
|
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Targeted capture and sequencing for detection of mutations causing early onset epileptic encephalopathy.
|
23662938 |
2013 |
rs866859766
|
RS1;CDKL5
|
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.
|
23708187 |
2013 |
rs866859766
|
RS1;CDKL5
|
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Targeted capture and sequencing for detection of mutations causing early onset epileptic encephalopathy.
|
23662938 |
2013 |
rs267608468
|
Entrez Id: |
6792 |
Gene Symbol: |
CDKL5 |
CDKL5
|
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
A novel mutation in the X-linked cyclin-dependent kinase-like 5 (CDKL5) gene associated with a severe Rett phenotype.
|
19253388 |
2009 |
rs267608468
|
Entrez Id: |
6792 |
Gene Symbol: |
CDKL5 |
CDKL5
|
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Novel mutations in the CDKL5 gene, predicted effects and associated phenotypes.
|
19241098 |
2009 |
rs267608493
|
Entrez Id: |
6792 |
Gene Symbol: |
CDKL5 |
CDKL5
|
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
A novel mutation in the X-linked cyclin-dependent kinase-like 5 (CDKL5) gene associated with a severe Rett phenotype.
|
19253388 |
2009 |
rs267608493
|
Entrez Id: |
6792 |
Gene Symbol: |
CDKL5 |
CDKL5
|
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Novel mutations in the CDKL5 gene, predicted effects and associated phenotypes.
|
19241098 |
2009 |
rs267608501
|
Entrez Id: |
6792 |
Gene Symbol: |
CDKL5 |
CDKL5
|
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2
|
|
0.700 |
GeneticVariation |
UNIPROT |
Novel mutations in the CDKL5 gene, predicted effects and associated phenotypes.
|
19241098 |
2009 |