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progressive myoclonic epilepsy
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
NHLRC1
SLC7A6OS
KCTD7
ASAH1
SMAJ
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
GSE26030_UNSTIM_VS_RESTIM_TH17_DAY15_POST_POLARIZATION_DN
GSE12392_WT_VS_IFNB_KO_CD8A_POS_SPLEEN_DC_UP
WU_CELL_MIGRATION
GSE40685_NAIVE_CD4_TCELL_VS_TREG_DN
GSE45365_NK_CELL_VS_CD8A_DC_UP
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Curated Studies
Most Correlated Studies
Mouse Phenotypes - Epilepsy
OMIM - Epilepsy Related Disorders
OMIM - Spinal muscular atrophy disorders
OMIM - Epilepsy disorders
OMIM - Ataxia
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Literature
Most Relevant Literature
Efficacy of topiramate as add-on therapy in two different types of progressive myoclonic epilepsy.
Novel mutation in potassium channel related gene KCTD7 and progressive myoclonic epilepsy.
Progressive myoclonic epilepsy.
Spinal muscular atrophy associated with progressive myoclonic epilepsy is caused by mutations in ASA…
3D texture analysis reveals imperceptible MRI textural alterations in the thalamus and putamen in pr…
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Clinical Trials
Most Relevant Clinical Trials
Effect of Ropinirole Hydrochloride in Progressive Myoclonic Epilepsy of Unverricht-Lundborg Type
Biology of Juvenile Myoclonic Epilepsy
Neocortical Epilepsies - Do They Progress?
Efficacy and Safety of GWP42003-P Oral Solution in Children With Epilepsy With Myoclonic-atonic Seiz…
Efficacy and Safety of Adjunctive Zonisamide in Myoclonic Seizures Associated With Idiopathic Genera…
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