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Article

What is new in CDG?

Journal of inherited metabolic disease - 1 Jul 2017

Jaeken Jaak, Péanne Romain

Abstract excerpt

Congenital disorders of glycosylation (CDG) are one group among the disorders of glycosylation. The latter comprise defects associated with hypoglycosylation but also defects with hyperglycosylation. Genetic diseases with hypoglycosylation can be divided in primary congenital disorders of glycosylation (CDG) and in genetic diseases causing secondary hypoglycosylation. This review covers the human CDG highlights...

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Source

Identifiers

PMID: 28484880
DOI: 10.1007/s10545-017-0050-6

Genes

ALG9
CAD
DHDDS
EXT2
FKRP
FKTN
GANAB
NANS
NUS1
PGAP1
PGAP3
PGM3
PIGA
PIGC
PIGG
PIGN
PIGW
PIGY
POGLUT1
SSR4
TRAPPC11
XYLT1
XYLT2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

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