Biallelic variants in the UTRN gene cause a novel form of multiple congenital arthrogryposis.

Melnik E, Akimova D, Markova T, Tatarskiy E, Tvorogova A, Zabnenkova V, Kenis V, Agranovich O, Skoblov M, Dadali E

DOI: 10.3389/fgene.2025.1664424
Published: 2025
Container: Frontiers in genetics
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. Source: Crossref; license: CC0 metadata
cautionDOI resolves: No matching Crossref record was present in this response. Source: Crossref; license: CC0 metadata
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. Source: DOAJ; license: CC0
not scoredMEDLINE indexed: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
not scoredOpenAlex core source: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
not scoredKnown publisher allow-list: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
not scoredROR affiliation: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
not scoredRetraction Watch retraction: No retraction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete. Source: Retraction Watch; license: CC BY 4.0
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. Source: Retraction Watch; license: CC BY 4.0
not scoredRetraction Watch correction: No correction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete. Source: Retraction Watch; license: CC BY 4.0
not scoredRetraction Watch reinstatement: No reinstatement notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete. Source: Retraction Watch; license: CC BY 4.0
supportingOpen access status: Normalized open-access status: open. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
not scoredPublication license: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
not scoredPublication version: A publication version was supplied but is not scored. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer

Cite this work

BibTeX

@article{allodium:10.3389/fgene.2025.1664424,
  title = {Biallelic variants in the UTRN gene cause a novel form of multiple congenital arthrogryposis.},
  author = {Melnik E and Akimova D and Markova T and Tatarskiy E and Tvorogova A and Zabnenkova V and Kenis V and Agranovich O and Skoblov M and Dadali E},
  year = {2025},
  journal = {Frontiers in genetics},
  doi = {10.3389/fgene.2025.1664424},
  url = {https://doi.org/10.3389/fgene.2025.1664424}
}

RIS

TY  - JOUR
TI  - Biallelic variants in the UTRN gene cause a novel form of multiple congenital arthrogryposis.
AU  - Melnik E
AU  - Akimova D
AU  - Markova T
AU  - Tatarskiy E
AU  - Tvorogova A
AU  - Zabnenkova V
AU  - Kenis V
AU  - Agranovich O
AU  - Skoblov M
AU  - Dadali E
PY  - 2025
JO  - Frontiers in genetics
DO  - 10.3389/fgene.2025.1664424
UR  - https://doi.org/10.3389/fgene.2025.1664424
ER  -

APA

E, M., D, A., T, M., E, T., A, T., V, Z., V, K., O, A., M, S., & E, D. (2025). Biallelic variants in the UTRN gene cause a novel form of multiple congenital arthrogryposis.. Frontiers in genetics. https://doi.org/10.3389/fgene.2025.1664424

Source records

pubmed · retrieved 2026-09-26T17:34:31.672Z