De novo mutations in GRIN1 cause extensive bilateral polymicrogyria. (2018)
Attributed to:
Computational Genomics Analysis and Training programme (CGAT)
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1093/brain/awx358
PubMed Identifier: 29365063
Publication URI: http://europepmc.org/abstract/MED/29365063
Type: Journal Article/Review
Volume: 141
Parent Publication: Brain : a journal of neurology
Issue: 3
ISSN: 0006-8950