BaseSpace
Correlation
Engine-Public
Sign In
Register
Correlation Engine 2.0
Home
My Data
Bookmarks
Collaborations
Inbox
Import Your Data
QuickView
FAQ
What is QuickView?
What can my QuickView results tell me?
What are the sources for the General Info tab in QuickView?
More QuickView FAQs
Back to top
QuickView
Curated
Studies
Body
Atlas
Disease
Atlas
Pharmaco
Atlas
Knockdown
Atlas
Genetic
Markers
Pathway
Enrichment
Literature
Clinical
Trials
0
Meta-
Analysis
QuickView
Search sequence regions
(e.g.
rs3825942
,
SNCA
,
glucose metabolic process
,
Obesity
,
Neuron
,
Early pregnancy factor
)
Organisms
Chromosomes
Start
Stop
Homo Sapiens
Mus Musculus
Rattus Norvegicus
C. Elegans
D. Melanogaster
Saccharomyces Cerevisiae
QuickView
Go back to main search
Bookmark
Forward
QuickView
for
myoclonic astatic epilepsy
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
No genes found
No SNPs found
Explore Genetic Markers Results
Pathway Enrichment
Most Correlated Biogroups
No biogroups found
Explore Pathway Enrichment Results
Curated Studies
Most Correlated Studies
No studies found
Explore Curated Studies Results
Literature
Most Relevant Literature
Dissecting the genetic basis of myoclonic-astatic epilepsy.
Myoclonic astatic epilepsy and the use of the ketogenic diet.
Myoclonic astatic epilepsy (Doose syndrome) - a lamotrigine responsive epilepsy?
Glucose transporter 1 deficiency as a treatable cause of myoclonic astatic epilepsy.
A patient with myoclonic epilepsy in infancy followed by myoclonic astatic epilepsy.
Explore Literature Results
Clinical Trials
Most Relevant Clinical Trials
Efficacy and Safety of GWP42003-P Oral Solution in Children With Epilepsy With Myoclonic-atonic Seiz…
Ketogenic Diet for New-Onset Absence Epilepsy
Modified Atkins Diet in Childhood Epilepsy
A Pilot Study of Efficacy and Tolerability of Levetiracetam Monotherapy in Subjects With Childhood A…
The Becoming of Children With Doose Syndrome
Explore Clinical Trials Results
search
→
result
search
→
result
See more about this page
See complete FAQ