Total loss of GM3 synthase activity by a normally processed enzyme in a novel variant and in all ST3GAL5 variants reported to cause a distinct congenital disorder of glycosylation
Indellicato, Rossella, Parini, Rossella, Domenighini, Ruben, Malagolini, Nadia, Iascone, Maria, Gasperini, Serena, Masera, Nicoletta, dall'Olio, Fabio, Trinchera, MarcoLanguage:
english
Journal:
Glycobiology
DOI:
10.1093/glycob/cwy112
Date:
December, 2018
File:
PDF, 4.12 MB
english, 2018