Translocation breakpoint at 7q31 associated with tics: further evidence for IMMP2L as a candidate gene for Tourette syndrome.
- DOI
- 10.1038/ejhg.2010.238
- Published
- 2011 Jun
- Container
- European journal of human genetics : EJHG
- 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:10.1038/ejhg.2010.238,
title = {Translocation breakpoint at 7q31 associated with tics: further evidence for IMMP2L as a candidate gene for Tourette syndrome.},
author = {Patel C and Cooper-Charles L and McMullan DJ and Walker JM and Davison V and Morton J},
year = {2011},
journal = {European journal of human genetics : EJHG},
doi = {10.1038/ejhg.2010.238},
url = {https://doi.org/10.1038/ejhg.2010.238}
}RIS
TY - JOUR TI - Translocation breakpoint at 7q31 associated with tics: further evidence for IMMP2L as a candidate gene for Tourette syndrome. AU - Patel C AU - Cooper-Charles L AU - McMullan DJ AU - Walker JM AU - Davison V AU - Morton J PY - 2011 JO - European journal of human genetics : EJHG DO - 10.1038/ejhg.2010.238 UR - https://doi.org/10.1038/ejhg.2010.238 ER -
APA
C, P., L, C., DJ, M., JM, W., V, D., & J, M. (2011). Translocation breakpoint at 7q31 associated with tics: further evidence for IMMP2L as a candidate gene for Tourette syndrome.. European journal of human genetics : EJHG. https://doi.org/10.1038/ejhg.2010.238
Source records
- pubmed · retrieved 2026-11-10T11:58:05.573Z