De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia. (2020)
Attributed to:
Molecular Genetic Studies of Schizophrenia
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1038/s41593-019-0565-2
PubMed Identifier: 31932766
Publication URI: http://europepmc.org/abstract/MED/31932766
Type: Journal Article/Review
Volume: 23
Parent Publication: Nature neuroscience
Issue: 2
ISSN: 1097-6256