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Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum-associated degradation pathway.
Genet Med. 2014 Oct;16(10):751-8. doi: 10.1038/gim.2014.22. Epub 2014 Mar 20.
Genet Med. 2014.
PMID: 24651605
Free PMC article.
Structural and biochemical studies of the C-terminal domain of mouse peptide-N-glycanase identify it as a mannose-binding module.
Zhou X, Zhao G, Truglio JJ, Wang L, Li G, Lennarz WJ, Schindelin H.
Zhou X, et al.
Proc Natl Acad Sci U S A. 2006 Nov 14;103(46):17214-9. doi: 10.1073/pnas.0602954103. Epub 2006 Nov 6.
Proc Natl Acad Sci U S A. 2006.
PMID: 17088551
Free PMC article.
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