The Coriell Institute for Medical Research is proud to announce the release of new samples representing N-glycanase deficiency, caused by a mutation on the NGLY 1 gene, also known as...
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Recent research in the NGLY1 community has been published on Nature.com. To read the entire journal article called “JOURNAL ARTICLE: Prospective phenotyping of NGLY1-CDDG, the first congenital disorder of deglycosylation”,…
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