Identification of two novel variants in ALG11 causing congenital disorder of glycosylation-Reference-Cited by-同舟云学术

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Identification of two novel variants in ALG11 causing congenital disorder of glycosylation

Published:2024-10 Issue: Volume:121 Page:235-242
ISSN:1059-1311
Container-title:Seizure: European Journal of Epilepsy
language:en
Short-container-title:Seizure: European Journal of Epilepsy

Author:

Zhao Peiwei,Zhang Xiankai,Duan Zhengrong,Wan Chunhui,Zhang Lei,Luo Sukun,Zhu Hongmin,He Xuelian^ORCID

Funder

Hubei Province Natural Science Foundation

Publisher

Elsevier BV

Reference32 articles.

1. Structural Basis of Glycan Diversity;Bertozzi,2009

2. Perspectives on Glycosylation and Its Congenital Disorders;Ng;Trends Genet,2018

3. Congenital disorders of glycosylation. Handb Clin Neurol 113: 1737–1743.

4. Recognizable phenotypes in CDG;Ferreira;J Inherit Metab Dis,2018

5. Freeze HH. Chemical Therapies for Congenital Disorders of Glycosylation;Sosicka;ACS Chem Biol,2022

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