Coagulation abnormalities and vascular complications are common in PGM1-CDG-Reference-Cited by-同舟云学术

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Coagulation abnormalities and vascular complications are common in PGM1-CDG

Published:2024-08 Issue:4 Volume:142 Page:108530
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Radenkovic Silvia,Bleukx Sofie,Engelhardt Nicole,Eklund Erik,Mercimek-Andrews Saadet,Edmondson Andrew C.,Morava Eva

Publisher

Elsevier BV

Reference48 articles.

1. Congenital Disorders of Glycosylation: A Multi-genetic Disease Family with Multiple Subcellular Locations;Jaeken,2020

2. Sialic Acid-Deficient Serum and Cerebrospinal Fluid Transferrin in a Newly Recognized Genetic Syndrome;Jaeken,1984

3. Congenital Disorders of Glycosylation;Jaeken,2013

4. Phenotypic and genotypic spectrum of congenital disorders of glycosylation type I and type II;Al Teneiji;Mol. Genet. Metab.,2017

5. How to Find and Diagnose a CDG due to Defective N-Glycosylation;Lefeber,2011

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