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
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Núria Queralt Rosinach, 8 Dec 2021, 21:44:54 UTC
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Núria Queralt Rosinach, 8 Dec 2021, 21:39:35 UTC
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Article: Data Science and symbolic AI: Synergies, challenges and opportunities DataScience PositionPaper ScholarlyWork
Robert Hoehndorf et al. (authors), Tobias Kuhn (creator), 5 May 2025, 09:13:17 UTC
NGLY1 deficiency is a novel autosomal recessive disorder of the ERAD pathway. DataScience SuperPatternInstance
Núria Queralt Rosinach (author), Tobias Kuhn (creator), 9 Apr 2025, 06:33:41 UTC