Common genetic variants contribute to risk of rare severe neurodevelopmental disorders. (2018)
Attributed to:
METADAC
funded by
ESRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1038/s41586-018-0566-4
PubMed Identifier: 30258228
Publication URI: http://europepmc.org/abstract/MED/30258228
Type: Journal Article/Review
Volume: 562
Parent Publication: Nature
Issue: 7726
ISSN: 0028-0836