Mechanism Identified for Rare Disorder of Glycosylation
Greenwood, SC (December 8, 2021) – Greenwood Genetic Center (GGC) researchers are reporting the discovery of a mechanism that contributes to the
Source: miragenews.com
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Researchers discover mechanism for congenital disorders of glycosylation
Greenwood Genetic Center researchers are reporting the discovery of a mechanism that contributes to the tissue phenotypes seen in PMM2-CDG, the most common of the congenital disorders of glycosylation (CDGs).
Source: news-medical.net