Exome sequencing reveals aggregates of rare variants in glycosyltransferase and other genes influencing immunoglobulin G and transferrin glycosylation (2022)
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/10.1101/2022.12.26.22283911
Publication URI: http://dx.doi.org/10.1101/2022.12.26.22283911
Type: Preprint