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Congenital disorders of glycosylation: A multi-genetic disease family with multiple subcellular locations Cover

Congenital disorders of glycosylation: A multi-genetic disease family with multiple subcellular locations

Journal of Mother and Child
Volume 24 (2020): Issue 2 (June 2020)
By: Jaak Jaeken  
Open Access
|Nov 2020

Authors

Jaak Jaeken

jaak.jaeken@kuleuven.be

Department of Development and Regeneration, Center for Metabolic Diseases, University Hospital Gasthuisberg, KU Leuven, Leuven, Belgium
DOI: https://doi.org/10.34763/jmotherandchild.20202402si.2005.000004 | Journal eISSN: 2719-535X | Journal ISSN: 2719-6488
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Language: English
Page range: 14 - 20
Published on: Nov 10, 2020
Published by: Institute of Mother and Child
In partnership with: Paradigm Publishing Services
Publication frequency: 1 issue per year
Keywords:
congenital disorders of glycosylation,
protein glycosylation defects,
N-glycosylation disorders,
O-glycosylation disorders,
cytosolic CDG,
endoplasmic reticulum-related CDG,
ER-related CDG,
ER–Golgi intermediate compartment (ERGIC) CDG,
plasma membrane,
sarcolemmal membrane
Related subjects:
Medicine,
Clinical medicine,
Pediatrics and juvenile medicine,
Paediatric haematology and oncology,
Public health

© 2020 Jaak Jaeken, published by Institute of Mother and Child
This work is licensed under the Creative Commons Attribution 4.0 License.

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