Mutations in OCRL1 gene in Indian children with Lowe syndrome.
- DOI
- 10.1007/s10157-008-0059-0
- Published
- 2008 Oct
- Container
- Clinical and experimental nephrology
- Publisher
- Not recorded
- Open access
- no
Credibility signals
limited evidence Score 43/100 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.
- not scoredOpen access status: Not checked or no result supplied; no credibility inference made.
- 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/s10157-008-0059-0,
title = {Mutations in OCRL1 gene in Indian children with Lowe syndrome.},
author = {Sethi SK and Bagga A and Gulati A and Hari P and Gupta N and Lunardi J},
year = {2008},
journal = {Clinical and experimental nephrology},
doi = {10.1007/s10157-008-0059-0},
url = {https://doi.org/10.1007/s10157-008-0059-0}
}RIS
TY - JOUR TI - Mutations in OCRL1 gene in Indian children with Lowe syndrome. AU - Sethi SK AU - Bagga A AU - Gulati A AU - Hari P AU - Gupta N AU - Lunardi J PY - 2008 JO - Clinical and experimental nephrology DO - 10.1007/s10157-008-0059-0 UR - https://doi.org/10.1007/s10157-008-0059-0 ER -
APA
SK, S., A, B., A, G., P, H., N, G., & J, L. (2008). Mutations in OCRL1 gene in Indian children with Lowe syndrome.. Clinical and experimental nephrology. https://doi.org/10.1007/s10157-008-0059-0
Source records
- pubmed · retrieved 2026-09-25T08:17:27.594Z
- europe-pmc · retrieved 2026-09-25T08:17:27.602Z
- hal · retrieved 2026-09-25T08:17:27.659Z