Epilepsy, Partial, with Variable Foci
|
0.770 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
|
|
|
Epilepsy, Partial, with Variable Foci
|
0.770 |
GermlineCausalMutation
|
disease |
ORPHANET |
Study of families with focal epilepsy that were too small for conventional clinical diagnosis with FFEVF identified DEPDC5 mutations in approximately 12% of families (10/82).
|
23542697 |
2013 |
Epilepsy, Partial, with Variable Foci
|
0.770 |
Biomarker
|
disease |
CLINGEN |
Study of families with focal epilepsy that were too small for conventional clinical diagnosis with FFEVF identified DEPDC5 mutations in approximately 12% of families (10/82).
|
23542697 |
2013 |
Epilepsy, Partial, with Variable Foci
|
0.770 |
GeneticVariation
|
disease |
CLINVAR |
Study of families with focal epilepsy that were too small for conventional clinical diagnosis with FFEVF identified DEPDC5 mutations in approximately 12% of families (10/82).
|
23542697 |
2013 |
Epilepsy, Partial, with Variable Foci
|
0.770 |
GeneticVariation
|
disease |
BEFREE |
Study of families with focal epilepsy that were too small for conventional clinical diagnosis with FFEVF identified DEPDC5 mutations in approximately 12% of families (10/82).
|
23542697 |
2013 |
Epilepsy, Partial, with Variable Foci
|
0.770 |
Biomarker
|
disease |
CTD_human |
Study of families with focal epilepsy that were too small for conventional clinical diagnosis with FFEVF identified DEPDC5 mutations in approximately 12% of families (10/82).
|
23542697 |
2013 |
Epilepsy, Partial, with Variable Foci
|
0.770 |
CausalMutation
|
disease |
CLINVAR |
Study of families with focal epilepsy that were too small for conventional clinical diagnosis with FFEVF identified DEPDC5 mutations in approximately 12% of families (10/82).
|
23542697 |
2013 |
Epilepsy, Partial, with Variable Foci
|
0.770 |
Biomarker
|
disease |
CLINGEN |
Mutations of DEPDC5 cause autosomal dominant focal epilepsies.
|
23542701 |
2013 |
Epilepsy, Partial, with Variable Foci
|
0.770 |
GermlineCausalMutation
|
disease |
ORPHANET |
Mutations of DEPDC5 cause autosomal dominant focal epilepsies.
|
23542701 |
2013 |
Epilepsy, Partial, with Variable Foci
|
0.770 |
CausalMutation
|
disease |
CLINVAR |
Mutations of DEPDC5 cause autosomal dominant focal epilepsies.
|
23542701 |
2013 |
Epilepsy, Partial, with Variable Foci
|
0.770 |
GeneticVariation
|
disease |
CLINVAR |
Mutations of DEPDC5 cause autosomal dominant focal epilepsies.
|
23542701 |
2013 |
Epilepsy, Partial, with Variable Foci
|
0.770 |
Biomarker
|
disease |
CTD_human |
Mutations of DEPDC5 cause autosomal dominant focal epilepsies.
|
23542701 |
2013 |
Epilepsy, Partial, with Variable Foci
|
0.770 |
Biomarker
|
disease |
CLINGEN |
Mutations in DEPDC5 have recently been identified in multiple cases of FFEVF as well as in a wide spectrum of other familial focal epilepsies.
|
24283814 |
2014 |
Epilepsy, Partial, with Variable Foci
|
0.770 |
GeneticVariation
|
disease |
BEFREE |
Mutations in DEPDC5 have recently been identified in multiple cases of FFEVF as well as in a wide spectrum of other familial focal epilepsies.
|
24283814 |
2014 |
Epilepsy, Partial, with Variable Foci
|
0.770 |
GeneticVariation
|
disease |
BEFREE |
We recently identified DEPDC5 as the gene for familial focal epilepsy with variable foci and found mutations in >10% of small families with nonlesional focal epilepsy.
|
24585383 |
2014 |
Epilepsy, Partial, with Variable Foci
|
0.770 |
CausalMutation
|
disease |
CLINVAR |
Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformations.
|
24585383 |
2014 |
Epilepsy, Partial, with Variable Foci
|
0.770 |
CausalMutation
|
disease |
CLINVAR |
DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsy.
|
24814846 |
2014 |
Epilepsy, Partial, with Variable Foci
|
0.770 |
GeneticVariation
|
disease |
BEFREE |
Small ADNFLE pedigrees with DEPDC5 mutations might actually represent a part of the broader familial focal epilepsy with variable foci phenotype.
|
24814846 |
2014 |
Epilepsy, Partial, with Variable Foci
|
0.770 |
CausalMutation
|
disease |
CLINVAR |
Familial cortical dysplasia type IIA caused by a germline mutation in DEPDC5.
|
26000329 |
2015 |
Epilepsy, Partial, with Variable Foci
|
0.770 |
GeneticVariation
|
disease |
BEFREE |
Mutations in the DEPDC5 (DEP domain-containing protein 5) gene are a major cause of familial focal epilepsy with variable foci (FFEVF) and are predicted to account for 12-37% of families with inherited focal epilepsies.
|
26216793 |
2015 |
Epilepsy, Partial, with Variable Foci
|
0.770 |
CausalMutation
|
disease |
CLINVAR |
Mutations in the mammalian target of rapamycin pathway regulators NPRL2 and NPRL3 cause focal epilepsy.
|
26505888 |
2016 |
Epilepsy, Partial, with Variable Foci
|
0.770 |
CausalMutation
|
disease |
CLINVAR |
Exome-based analysis of cardiac arrhythmia, respiratory control, and epilepsy genes in sudden unexpected death in epilepsy.
|
26704558 |
2016 |
Epilepsy, Partial, with Variable Foci
|
0.770 |
CausalMutation
|
disease |
CLINVAR |
Epileptic spasms are a feature of DEPDC5 mTORopathy.
|
27066554 |
2015 |
Epilepsy, Partial, with Variable Foci
|
0.770 |
CausalMutation
|
disease |
CLINVAR |
Ultra-rare genetic variation in common epilepsies: a case-control sequencing study.
|
28102150 |
2017 |
Epilepsy, Partial, with Variable Foci
|
0.770 |
CausalMutation
|
disease |
CLINVAR |
Real-world utility of whole exome sequencing with targeted gene analysis for focal epilepsy.
|
28199897 |
2017 |