Identification of homozygous missense variant in SIX5 gene underlying recessive nonsyndromic hearing impairment.
- DOI
- 10.1371/journal.pone.0268078
- Published
- 2022
- Container
- PloS one
- Publisher
- Not recorded
- Open access
- yes
Credibility signals
uncertain Score 53/100 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.
- supportingDirectory of Open Access Journals: A matching record was returned by DOAJ.
- 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:10.1371/journal.pone.0268078,
title = {Identification of homozygous missense variant in SIX5 gene underlying recessive nonsyndromic hearing impairment.},
author = {Kakar MU and Akram M and Zubair Mehboob M and Younus M and Bilal M and Waqas A and Nazir A and Shafi M and Umair M and Ahmad S and Rafeeq MM},
year = {2022},
journal = {PloS one},
doi = {10.1371/journal.pone.0268078},
url = {https://doi.org/10.1371/journal.pone.0268078}
}RIS
TY - JOUR TI - Identification of homozygous missense variant in SIX5 gene underlying recessive nonsyndromic hearing impairment. AU - Kakar MU AU - Akram M AU - Zubair Mehboob M AU - Younus M AU - Bilal M AU - Waqas A AU - Nazir A AU - Shafi M AU - Umair M AU - Ahmad S AU - Rafeeq MM PY - 2022 JO - PloS one DO - 10.1371/journal.pone.0268078 UR - https://doi.org/10.1371/journal.pone.0268078 ER -
APA
MU, K., M, A., M, Z. M., M, Y., M, B., A, W., A, N., M, S., M, U., S, A., & MM, R. (2022). Identification of homozygous missense variant in SIX5 gene underlying recessive nonsyndromic hearing impairment.. PloS one. https://doi.org/10.1371/journal.pone.0268078