Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis. (2016)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1136/jmedgenet-2015-103263
PubMed Identifier: 26993267
Publication URI: http://europepmc.org/abstract/MED/26993267
Type: Journal Article/Review
Volume: 53
Parent Publication: Journal of medical genetics
Issue: 5
ISSN: 0022-2593