Publications
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[ Author] Title Year Filters: Author is Ng, Bobby G and Keyword is Glycosylation [Clear All Filters]
Mosaicism of the UDP-galactose transporter SLC35A2 causes a congenital disorder of glycosylation. Am J Hum Genet 92, 632-6 (2013).
ALG1-CDG: Clinical and Molecular Characterization of 39 Unreported Patients. Hum Mutat 37, 653-60 (2016).