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Document type:
Article; Journal Article
Author(s):
Hüllen, Andreas; Falkenstein, Kristina; Weigel, Corina; Huidekoper, Hidde; Naumann-Bartsch, Nora; Spenger, Johannes; Feichtinger, René G; Schaefers, Jacqueline; Frenz, Stephanie; Kotlarz, Daniel; Momen, Tooba; Khoshnevisan, Razieh; Riedhammer, Korbinian M; Santer, René; Herget, Theresia; Rennings, Alexander; Lefeber, Dirk J; Mayr, Johannes A; Thiel, Christian; Wortmann, Saskia B
Title:
Congenital disorders of glycosylation with defective fucosylation.
Abstract:
Fucosylation is essential for intercellular and intracellular recognition, cell-cell interaction, fertilization, and inflammatory processes. Only five types of congenital disorders of glycosylation (CDG) related to an impaired fucosylation have been described to date: FUT8-CDG, FCSK-CDG, POFUT1-CDG SLC35C1-CDG, and the only recently described GFUS-CDG. This review summarizes the clinical findings of all hitherto known 25 patients affected with those defects with regard to their pathophysiology a...     »
Journal title abbreviation:
J Inherit Metab Dis
Year:
2021
Journal volume:
44
Journal issue:
6
Pages contribution:
1441-1452
Fulltext / DOI:
doi:10.1002/jimd.12426
Pubmed ID:
http://view.ncbi.nlm.nih.gov/pubmed/34389986
Print-ISSN:
0141-8955
TUM Institution:
Fachgebiet Nephrologie (Prof. Heemann); Institut für Humangenetik
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