Full identifier: https://orcid.org/0000-0003-0169-8159
NGLY1 deficiency is a novel autosomal recessive disorder of the ERAD pathway. SuperPatternInstance
Núria Queralt Rosinach, 17 Dec 2021, 09:26:28 UTC
Dysfunction of ERAD pathway Class
Núria Queralt Rosinach, 17 Dec 2021, 09:19:45 UTC
RAT7nWZzE2 AgreementComment ResponseComment PointAddressedComment
Núria Queralt Rosinach, 8 Dec 2021, 21:46:32 UTC
RA4H1CPJ7Y AgreementComment ResponseComment PointAddressedComment
Núria Queralt Rosinach, 8 Dec 2021, 21:44:54 UTC
RAxkzPSjaG PartialAgreementComment ResponseComment PointAddressedComment
Núria Queralt Rosinach, 8 Dec 2021, 21:39:35 UTC
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