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CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ii
Known as:
CDG1I
, Congenital disorder of glycosylation type II
, CDG Ii
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National Institutes of Health
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Related topics
Related topics
10 relations
ALG2 gene
Autosomal recessive inheritance
Cataract
Congenital disorder of glycosylation type 2E
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Broader (1)
Congenital Disorders of Glycosylation
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
MAN 1 B 1 Deficiency : An Unexpected CDG-II
D. Rymen
,
Romain Péanne
,
+15 authors
G. Matthijs
2014
Corpus ID: 171084885
Congenital disorders of glycosylation (CDG) are a group of rare metabolic diseases, due to impaired protein and lipid…
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Review
2006
Review
2006
O-glycosylation in health and disease
S. Wopereis
2006
Corpus ID: 58432135
Background: Genetic diseases that affect the biosynthesis of protein O-glycans are a rapidly growing group of disorders. Because…
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