Clinical whole-genome sequencing in severe early-onset epilepsy reveals new genes and improves molecular diagnosis. (2014)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1093/hmg/ddu030
PubMed Identifier: 24463883
Publication URI: http://europepmc.org/abstract/MED/24463883
Type: Journal Article/Review
Volume: 23
Parent Publication: Human molecular genetics
Issue: 12
ISSN: 0964-6906