S-sulfocysteine/NMDA receptor–dependent signaling underlies neurodegeneration in molybdenum cofactor deficiency
Author:
Funder
Center for Molecular Medicine Cologne
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Link
https://www.jci.org/articles/view/89885/files/pdf
Reference49 articles.
1. Inborn errors of molybdenum metabolism: combined deficiencies of sulfite oxidase and xanthine dehydrogenase in a patient lacking the molybdenum cofactor.
2. Combined deficiency of xanthine oxidase and sulphite oxidase: A defect of molybdenum metabolism or transport?
3. Molybdenum cofactor deficiency: Mutations in GPHN, MOCS1, and MOCS2
4. Molybdenum cofactor deficiency: Review of 12 cases (MoCD and review)
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