Associated Papers
Fractionated plasma N-glycan profiling of novel cohort of ATP6AP1-CDG subjects identifies phenotypic association.
Alharbi H et al.
Journal of Inherited Metabolic Disease, 2023
Congenital disorder of glycosylation caused by mutation of ATP6AP1 gene (c.1036G>A) in a Chinese infant: A case report.
Yang X et al.
World Journal of Clinical Cases, 2021
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