Associated Papers
Clinical and genetic characterization of congenital disorders of glycosylation in 20 Chinese patients.
Zhao P et al.
Orphanet Journal of Rare Diseases, 2025
Updated clinical and glycomic features of mannosyl-oligosaccharide glucosidase deficiency: Two case reports.
Abuduxikuer K et al.
World Journal of Clinical Cases, 2022
Clinical, biochemical and genetic characteristics of MOGS-CDG: a rare congenital disorder of glycosylation.
Shimada S et al.
Journal of Medical Genetics, 2022
Identification and characterization of novel mutations in MOGS in a Chinese patient with infantile spams.
Peiwei Zhao et al.
Neurogenetics, 2020
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