Laddar...

ExACtly zero or once: A clinically helpful guide to assessing genetic variants in mild epilepsies

OBJECTIVE: To assist the interpretation of genomic data for common epilepsies, we asked whether variants implicated in mild epilepsies in autosomal dominant families are present in the general population. METHODS: We studied 12 genes for the milder epilepsies and identified published variants with s...

Full beskrivning

Sparad:
Bibliografiska uppgifter
I publikationen:Neurol Genet
Huvudupphovsmän: Bennett, Caitlin A., Petrovski, Slavé, Oliver, Karen L., Berkovic, Samuel F.
Materialtyp: Artigo
Språk:Inglês
Publicerad: Wolters Kluwer 2017
Ämnen:
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC5503456/
https://ncbi.nlm.nih.gov/pubmed/28717674
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/NXG.0000000000000163
Taggar: Lägg till en tagg
Inga taggar, Lägg till första taggen!