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Congenital Disorders of Glycosylation: Clinical and Molecular Studies

Stephanie Grünewald
Stephanie Grünewald

Publication date

October 2016

Abstract

The following full text is a publisher's version. For additional information about this publication click this link

Extracted data

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Available from British Library Document Supply Centre- DSC:DXN060989 / BLDSC - British Library Docum...

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Frank, C.G.
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Clayton, P.T.
Winchester, B.G.
Smeitink, J.A.M.
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Matthijs, G.

January 2004

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Freeze, H.H.
Steet, R.
Kinoshita, T.
Varki, A.
Cummings, R.D.
Esko, J.D.
Stanley, P.
Hart, G.W.
Aebi, M.
Mohnen, D.
Kinoshita, T.
Packer, N.H.
Prestegard, J.H.
Schnaar, R.L.
Seeberger, P.H.

January 2022

This chapter discusses inherited human diseases that are caused by defects in glycan biosynthesis an...

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Morava, Eva
Witters, Peter

January 2016

Glycosylation is the most important posttranslational change for proteins. There are more than 100 d...

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Unalp, Aycan
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Kose, Engin
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January 2020

Objective: Congenital defects of glycosylation (CDG) belongs to a group of genetic diseases that lea...

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AbuBakar, N. Bin
Lefeber, D.J.
Scherpenzeel, M. van

January 2018

Contains fulltext : 191891.pdf (publisher's version ) (Open Access

Keeping an eye on congenital disorders of O-glycosylation: A systematic literature review

Francisco, Rita
Pascoal, Carlota
Marques-da-Silva, Dorinda
Morava, Eva
Gole, Glen A
Coman, David
Jaeken, Jaak
dos Reis Ferreira, Vanessa

January 2019

Congenital disorders of glycosylation (CDG) are a rapidly growing family comprising >100 genetic dis...

Congenital disorders of glycosylation: a concise chart of glycocalyx dysfunction

Hennet, Thierry
Cabalzar, Jürg

July 2015

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