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Common genetic variants contribute to risk of rare severe neurodevelopmental disorders. (2018)

First Author: Niemi MEK

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