Home
About
Overview
Sharing Data
ORCID
Help
History (0)
Find People
Find Everything
Login
to edit your profile (add a photo, awards, links to other websites, etc.)
Edit My Profile
My Person List (
0
)
Return to Top
Search Result Details
Back to Search Results
This page shows the details of why an item matched the keywords from your search.
Search Results
Rasmussen, Astrid
One or more keywords matched the following items that are connected to
Rasmussen, Astrid
Item Type
Name
Concept
Epilepsies, Myoclonic
Concept
Myoclonic Epilepsy, Juvenile
Academic Article
Recent developments in the quest for myoclonic epilepsy genes.
Academic Article
Mutations in EFHC1 cause juvenile myoclonic epilepsy.
Academic Article
DNA variants in coding region of EFHC1: SNPs do not associate with juvenile myoclonic epilepsy.
Academic Article
Genotype-phenotype correlations for EPM2A mutations in Lafora's progressive myoclonus epilepsy: exon 1 mutations associate with an early-onset cognitive deficit subphenotype.
Academic Article
Identification and mutational analysis of candidate genes for juvenile myoclonic epilepsy on 6p11-p12: LRRC1, GCLC, KIAA0057 and CLIC5.
Academic Article
Juvenile myoclonic epilepsy: linkage to chromosome 6p12 in Mexico families.
Academic Article
Mutation analyses of genes on 6p12-p11 in patients with juvenile myoclonic epilepsy.
Search Criteria
Epilepsies Myoclonic