(Q48678935)

English

On the nomenclature of congenital disorders of glycosylation (CDG).

scientific article published on 24 October 2008

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/18949576

On the nomenclature of congenital disorders of glycosylation (CDG). (English)

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/18949576

1 reference

based on heuristic

inferred from title

Hudson H. Freeze

3

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/18949576

author name string

J Jaeken

1

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/18949576

T Hennet

2

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/18949576

G Matthijs

4

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/18949576

publication date

24 October 2008

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/18949576

Journal of Inherited Metabolic Disease

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/18949576

31

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/18949576

6

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/18949576

669-672

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/18949576

Carbohydrate-deficient glycoprotein syndromes become congenital disorders of glycosylation: an updated nomenclature for CDG. First International Workshop on CDGS.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18949576

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital Disorders of Glycosylation: CDG-I, CDG-II, and beyond

1 reference

https://pubmed.ncbi.nlm.nih.gov/18949576

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infantile-onset symptomatic epilepsy syndrome caused by a homozygous loss-of-function mutation of GM3 synthase.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18949576

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital disorders of glycosylation

1 reference

https://pubmed.ncbi.nlm.nih.gov/18949576

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital disorders of glycosylation: a rapidly expanding disease family

1 reference

https://pubmed.ncbi.nlm.nih.gov/18949576

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carbohydrate deficient glycoprotein syndrome type II: a deficiency in Golgi localised N-acetyl-glucosaminyltransferase II.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18949576

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A defect in dolichol phosphate biosynthesis causes a new inherited disorder with death in early infancy

1 reference

https://pubmed.ncbi.nlm.nih.gov/18949576

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10545-008-0983-X

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/18949576

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 February 2018

http://europepmc.org/abstract/MED/18949576

ResearchGate publication ID

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