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ISGylation is disrupted by UBA7 gene variants identified in individuals with neurodevelopmental disorder phenotypes — Europe PMC PMID:42023152

Source
Europe PMC (en)
Original
https://europepmc.org/article/MED/42023152
DOI
10.1016/j.isci.2026.115454
License (as archived)
solo-consultazione
Archived
2026-11-03T15:54:34.663Z
SHA-256 of the archived text
ff670f34411348f3513dd929d0bb097a8792cba2f3af4c88c4f8425d1508b03d
Stable URL of this page
https://metraipolis.com/documento/dc_7199fc790deb

How to cite

ISGylation is disrupted by UBA7 gene variants identified in individuals with neurodevelopmental disorder phenotypes — Europe PMC PMID:42023152 — Europe PMC (en), https://europepmc.org/article/MED/42023152 (solo-consultazione); archived copy: https://metraipolis.com/documento/dc_7199fc790deb (Metraipolis archive dc_7199fc790deb, sha256 ff670f34411348f3513dd929d0bb097a8792cba2f3af4c88c4f8425d1508b03d)
BibTeX
@misc{dc7199fc790deb,
  title = {ISGylation is disrupted by UBA7 gene variants identified in individuals with neurodevelopmental disorder phenotypes — Europe PMC PMID:42023152},
  howpublished = {Europe PMC (en)},
  url = {https://europepmc.org/article/MED/42023152},
  note = {License solo-consultazione; archived copy https://metraipolis.com/documento/dc_7199fc790deb; sha256 ff670f34411348f3513dd929d0bb097a8792cba2f3af4c88c4f8425d1508b03d},
  year = {2026}
}

Archived text

The text is not reproduced here: the archive holds it as solo-consultazione (consultation only, no republication). Read it at the original source: https://europepmc.org/article/MED/42023152. Agents can read the archived copy with the MCP tool read_document.