The c.1744G > C, p.(Glu582Gln) missense variant in coding exon 14 of APC increases skipping of a natural occurring isoform and causes Familial Adenomatous Polyposis.
- DOI
- 10.1007/s00432-025-06357-w
- Published
- 2025 Dec 2
- Container
- Journal of cancer research and clinical oncology
- Publisher
- Not recorded
- Open access
- yes
Credibility signals
limited evidence Score 45/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.
Show all credibility signals
- cautionDOI registered: No matching Crossref record was present in this response.
- cautionDOI resolves: No matching Crossref record was present in this response.
- not scoredDirectory of Open Access Journals: No matching DOAJ record was present in this response. No allow-list match; this is not evidence of low credibility.
- not scoredMEDLINE indexed: Not checked or no result supplied; no credibility inference made.
- not scoredOpenAlex core source: Not checked or no result supplied; no credibility inference made.
- not scoredKnown publisher allow-list: Not checked or no result supplied; no credibility inference made.
- not scoredROR affiliation: Not checked or no result supplied; no credibility inference made.
- not scoredRetraction Watch retraction: No retraction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredRetraction Watch expression of concern: No expression of concern notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredRetraction Watch correction: No correction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredRetraction Watch reinstatement: No reinstatement notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- supportingOpen access status: Normalized open-access status: open.
- not scoredPublication license: Not checked or no result supplied; no credibility inference made.
- not scoredPublication version: A publication version was supplied but is not scored.
- cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty.
Cite this work
BibTeX
@article{allodium:10.1007/s00432-025-06357-w,
title = {The c.1744G > C, p.(Glu582Gln) missense variant in coding exon 14 of APC increases skipping of a natural occurring isoform and causes Familial Adenomatous Polyposis.},
author = {Jelsig AM and Boelman MB and Birkedal U and Hübertz J and Al-Zehawi L and Lautrup C and Karstensen JG and van Overeem Hansen T},
year = {2025},
journal = {Journal of cancer research and clinical oncology},
doi = {10.1007/s00432-025-06357-w},
url = {https://doi.org/10.1007/s00432-025-06357-w}
}RIS
TY - JOUR TI - The c.1744G > C, p.(Glu582Gln) missense variant in coding exon 14 of APC increases skipping of a natural occurring isoform and causes Familial Adenomatous Polyposis. AU - Jelsig AM AU - Boelman MB AU - Birkedal U AU - Hübertz J AU - Al-Zehawi L AU - Lautrup C AU - Karstensen JG AU - van Overeem Hansen T PY - 2025 JO - Journal of cancer research and clinical oncology DO - 10.1007/s00432-025-06357-w UR - https://doi.org/10.1007/s00432-025-06357-w ER -
APA
AM, J., MB, B., U, B., J, H., L, A., C, L., JG, K., & T, V. O. H. (2025). The c.1744G > C, p.(Glu582Gln) missense variant in coding exon 14 of APC increases skipping of a natural occurring isoform and causes Familial Adenomatous Polyposis.. Journal of cancer research and clinical oncology. https://doi.org/10.1007/s00432-025-06357-w
Source records
- pubmed · retrieved 2026-09-25T00:30:17.527Z