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What Is The Cause Of Type 2 Congenital Disorder Of Glycosylation? [Solved]
Congenital disorders of glycosylation These rare type II CDGs occur due to abnormal retrograde protein trafficking between Golgi apparatus and ER, therefore disrupt multiple glycosylation pathways that are associated with Golgi apparati.
Congenital Disorders of Glycosylation
In this module, Dr. Barbara Triggs-Raine, Professor at the University of Manitoba, will take the audience to examine the diverse …
What is PMM2-CDG?
Learn about the underlying biology of
Novel congenital disorder of O-linked glycosylation caused by GALNT2 loss of function
READ THE PAPER: https://bit.ly/2z5HlhA Zilmer et al. identify a novel
