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De novo mutations in GRIN1 cause extensive bilateral polymicrogyria. (2018)

First Author: Fry AE

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