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Exome sequencing reveals aggregates of rare variants in glycosyltransferase and other genes influencing immunoglobulin G and transferrin glycosylation (2022)

First Author: Landini A

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