CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1. (2014)
Attributed to:
MRC Centre for Neuropsychiatric Genetics and Genomics
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1093/hmg/ddt540
PubMed Identifier: 24163246
Publication URI: http://europepmc.org/abstract/MED/24163246
Type: Journal Article/Review
Volume: 23
Parent Publication: Human molecular genetics
Issue: 6
ISSN: 0964-6906