Prospective Phenotyping of NGLY1-CDDG, the First Congenital Disorder of Deglycosylation

PURPOSE: The cytosolic enzyme N-glycanase 1, encoded by NGLY1, catalyzes cleavage of the beta-aspartyl glycosylamine bond of N-linked glycoproteins, releasing intact N-glycans from proteins bound for degradation. In this study, we describe the clinical spectrum of NGLY1 deficiency (NGLY1-CDDG). METH...

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Gepubliceerd in:Genet Med
Hoofdauteurs: Lam, Christina, Ferreira, Carlos, Krasnewich, Donna, Toro, Camillo, Latham, Lea, Zein, Wadih M., Lehky, Tanya, Brewer, Carmen, Baker, Eva H., Thurm, Audrey, Farmer, Cristan A., Rosenzweig, Sergio D., Lyons, Jonathan J., Schreiber, John M., Gropman, Andrea, Lingala, Shilpa, Ghany, Marc G., Solomon, Beth, Macnamara, Ellen, Davids, Mariska, Stratakis, Constantine A., Kimonis, Virginia, Gahl, William A., Wolfe, Lynne
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 2016
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Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7477955/
https://ncbi.nlm.nih.gov/pubmed/27388694
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/gim.2016.75
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