A Novel Missense Variant in the Gene PPP2R5D Causes a Rare Neurodevelopmental Disorder with Increased Phenotype.
- DOI
- 10.1155/2021/6661860
- Published
- 2021
- Container
- BioMed research international
- Publisher
- Not recorded
- Open access
- yes
Credibility signals
serious concern Score 10/100 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.
- serious concernRetraction Watch retraction: 1 retraction notice matched this DOI.
- 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:10.1155/2021/6661860,
title = {A Novel Missense Variant in the Gene PPP2R5D Causes a Rare Neurodevelopmental Disorder with Increased Phenotype.},
author = {Yan L and Shen R and Cao Z and Han C and Zhang Y and Liu Y and Yang X and Xie M and Li H},
year = {2021},
journal = {BioMed research international},
doi = {10.1155/2021/6661860},
url = {https://doi.org/10.1155/2021/6661860}
}RIS
TY - JOUR TI - A Novel Missense Variant in the Gene PPP2R5D Causes a Rare Neurodevelopmental Disorder with Increased Phenotype. AU - Yan L AU - Shen R AU - Cao Z AU - Han C AU - Zhang Y AU - Liu Y AU - Yang X AU - Xie M AU - Li H PY - 2021 JO - BioMed research international DO - 10.1155/2021/6661860 UR - https://doi.org/10.1155/2021/6661860 ER -
APA
L, Y., R, S., Z, C., C, H., Y, Z., Y, L., X, Y., M, X., & H, L. (2021). A Novel Missense Variant in the Gene PPP2R5D Causes a Rare Neurodevelopmental Disorder with Increased Phenotype.. BioMed research international. https://doi.org/10.1155/2021/6661860
Source records
- pubmed · retrieved 2026-09-25T05:00:51.771Z