Defining the genetic control of human blood plasma N-glycome using genome-wide association study. (2019)
Attributed to:
Determining the causal links and clinical significance of rare genetic variants
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1093/hmg/ddz054
PubMed Identifier: 31163085
Publication URI: http://europepmc.org/abstract/MED/31163085
Type: Journal Article/Review
Volume: 28
Parent Publication: Human molecular genetics
Issue: 12
ISSN: 0964-6906