NGLY1 deficiency is a novel autosomal recessive disorder of the ERAD pathway.

Full identifier: http://purl.org/np/RASPvPrnUq6SOsOkrgOsUvRbsfmC7dHd73FgUA6oRmlGg

 NGLY1 deficiency is a novel autosomal recessive disorder of the ERAD pathway. SuperPatternInstance ▼ comment approve/disapprove edit as derived nanopublication create new with same template

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This is a local identifier that was minted when the nanopublication was created. http://purl.org/np/RASPvPrnUq...#activity activity http://www.w3.org/ns/prov#used used https://dx.doi.org/10.1038%2Fgim.2014.22 10.1038/gim.2014.22 .

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Núria Queralt Rosinach, 8 Dec 2021, 15:48:24 UTC

References