Associated Papers
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
Mannosyl-oligosaccharide glucosidase - congenital disorder of glycosylation: A patient with novel variants.
Ota M et al.
Pediatrics International : Official Journal of the Japan Pediatric Society, 2020
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