Severe infantile epileptic encephalopathy due to mutations in PLCB1: expansion of the genotypic and phenotypic disease spectrum. (2014)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1111/dmcn.12450
PubMed Identifier: 24684524
Publication URI: http://europepmc.org/abstract/MED/24684524
Type: Journal Article/Review
Volume: 56
Parent Publication: Developmental medicine and child neurology
Issue: 11
ISSN: 0012-1622