Dec 8, 2021
Researchers on the Greenwood Genetic Center (GGC) report the invention of a mechanism that contributes to the tissue phenotypes seen in PMM2-CDG, the commonest of the congenital glycosylation problems (CDGs). CDGs are a gaggle of over 130 uncommon genetic ailments brought on by defects within the glycosylation of lipids and proteins. The phenotypes are variable, …
Researchers discover mechanism for congenital glycosylation disorders https://psoec.com/researchers-discover-mechanism-for-congenital-glycosylation-disorders/?feed_id=1700&_unique_id=61b130c58a7c6