Keyword Connections

congenital disorders of glycosylation

Journals

1

1 human mutation

Research Groups

0

No Research Group Connected

Bibliographies

3

1 Novel variants and clinical symptoms in four new ALG3-CDG patients, review of the literature, and identification of AAGRP-ALG3 as a novel ALG3 variant with alanine and glycine-rich N-terminus.

2 bridging the gap between glycosylation and vesicle traffic

3 Glycosyltransferase genes that cause monogenic congenital disorders of glycosylation are distinct from glycosyltransferase genes associated with complex diseases