Identification of new risk factors for rolandic epilepsy: CNV at Xp22.31 and alterations at cholinergic synapses. (2018)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1136/jmedgenet-2018-105319
PubMed Identifier: 29789371
Publication URI: http://europepmc.org/abstract/MED/29789371
Type: Journal Article/Review
Volume: 55
Parent Publication: Journal of medical genetics
Issue: 9
ISSN: 0022-2593