(Q31030503)

28 June 2017

Congenital disorder of glycosylation (CDG) Ig: report on a patient and review of the literature (English)

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congenital disorder of glycosylation

28 June 2017

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Di Rocco M

1

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28 June 2017

Hennet T

2

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28 June 2017

Grubenmann CE

3

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28 June 2017

Pagliardini S

4

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28 June 2017

Allegri AE

5

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28 June 2017

Frank CG

6

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28 June 2017

Aebi M

7

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28 June 2017

Vignola S

8

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28 June 2017

Jaeken J

9

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28 June 2017

1 January 2005

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Journal of Inherited Metabolic Disease

28 June 2017

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28 June 2017

28

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28 June 2017

6

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28 June 2017

1162-1164

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https://scigraph.springernature.com/pub.10.1007/s10545-005-0137-3

28 June 2017

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cites work

Molecular and clinical description of the first US patients with congenital disorder of glycosylation Ig.

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12 December 2020

Abnormal glycosylation of red cell membrane band 3 in the congenital disorder of glycosylation Ig.

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12 December 2020

Congenital disorders of glycosylation type Ig is defined by a deficiency in dolichyl-P-mannose:Man7GlcNAc2-PP-dolichyl mannosyltransferase

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12 December 2020

Deficiency of dolichyl-P-Man:Man7GlcNAc2-PP-dolichyl mannosyltransferase causes congenital disorder of glycosylation type Ig

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12 December 2020

ALG12 mannosyltransferase defect in congenital disorder of glycosylation type lg

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12 December 2020

10.1007/S10545-005-0137-3

Identifiers

DOI

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Dimensions Publication ID

28 June 2017

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1 reference