SLC37A4-CDG: Mislocalization of the glucose-6-phosphate transporter to the Golgi causes a new congenital disorder of glycosylation-Reference-Cited by-同舟云学术

SLC37A4-CDG: Mislocalization of the glucose-6-phosphate transporter to the Golgi causes a new congenital disorder of glycosylation

Published:2020-12 Issue: Volume:25 Page:100636
ISSN:2214-4269
Container-title:Molecular Genetics and Metabolism Reports
language:en
Short-container-title:Molecular Genetics and Metabolism Reports

Author:

Marquardt Thorsten,Bzduch Vladimir,Hogrebe Max,Rust Stephan,Reunert Janine,Grüneberg Marianne,Park Julien,Callewaert Nico,Lachmann Robin,Wada Yoshinao,Engel Thomas

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology

Reference10 articles.

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3. Type I glycogen storage diseases: disorders of the glucose-6-phosphatase/glucose-6-phosphate transporter complexes;Chou;J. Inherit. Metab. Dis.,2015

4. Retention mechanisms for ER and Golgi membrane proteins;Gao;Trends Plant Sci.,2014

5. Limitations of galactose therapy in phosphoglucomutase 1 deficiency;Nolting;Mol. Genet. Metab. Rep.,2017

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1. The evolving genetic landscape of congenital disorders of glycosylation;Biochimica et Biophysica Acta (BBA) - General Subjects;2021-11

2. SLC37A4-CDG: New biochemical insights for an emerging congenital disorder of glycosylation with major coagulopathy;Clinica Chimica Acta;2021-10

3. A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction;The American Journal of Human Genetics;2021-06

4. Congenital disorder of glycosylation type II: Case report;Annals of Clinical and Analytical Medicine;2021

5. Novel Insights into Selected Disease-Causing Mutations within the SLC35A1 Gene Encoding the CMP-Sialic Acid Transporter;International Journal of Molecular Sciences;2020-12-30