Identification of common genetic risk variants for autism spectrum disorder. (2019)

First Author: Grove J
Attributed to:  Mendelian randomization to hypothesis-free causal inference funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41588-019-0344-8

PubMed Identifier: 30804558

Publication URI: http://europepmc.org/abstract/MED/30804558

Type: Journal Article/Review

Volume: 51

Parent Publication: Nature genetics

Issue: 3

ISSN: 1061-4036