hnRNPA2B1 and hnRNPA1 mutations are rare in patients with “multisystem proteinopathy” and frontotemporal lobar degeneration phenotypes
- DOI
- 10.1016/j.neurobiolaging.2013.09.016
- Published
- 2014-04
- Container
- Neurobiology of Aging
- Publisher
- Elsevier BV
- Open access
- unknown
Credibility signals
uncertain Score 64/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.
Show all credibility signals
- supportingDOI registered: A matching record was returned by Crossref.
- supportingDOI resolves: A matching record was returned by Crossref.
- 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.
- supportingMetadata completeness: All 6 scored descriptive metadata groups are present.
Cite this work
BibTeX
@article{allodium:10.1016/j.neurobiolaging.2013.09.016,
title = {hnRNPA2B1 and hnRNPA1 mutations are rare in patients with “multisystem proteinopathy” and frontotemporal lobar degeneration phenotypes},
author = {Isabelle Le Ber and Inge Van Bortel and Gael Nicolas and Kawtar Bouya-Ahmed and Agnès Camuzat and David Wallon and Anne De Septenville and Morwena Latouche and Serena Lattante and Edor Kabashi and Ludmila Jornea and Didier Hannequin and Alexis Brice},
year = {2014},
journal = {Neurobiology of Aging},
doi = {10.1016/j.neurobiolaging.2013.09.016},
url = {https://doi.org/10.1016/j.neurobiolaging.2013.09.016}
}RIS
TY - JOUR TI - hnRNPA2B1 and hnRNPA1 mutations are rare in patients with “multisystem proteinopathy” and frontotemporal lobar degeneration phenotypes AU - Isabelle Le Ber AU - Inge Van Bortel AU - Gael Nicolas AU - Kawtar Bouya-Ahmed AU - Agnès Camuzat AU - David Wallon AU - Anne De Septenville AU - Morwena Latouche AU - Serena Lattante AU - Edor Kabashi AU - Ludmila Jornea AU - Didier Hannequin AU - Alexis Brice PY - 2014 JO - Neurobiology of Aging DO - 10.1016/j.neurobiolaging.2013.09.016 UR - https://doi.org/10.1016/j.neurobiolaging.2013.09.016 ER -
APA
Ber, I. L., Bortel, I. V., Nicolas, G., Bouya-Ahmed, K., Camuzat, A., Wallon, D., Septenville, A. D., Latouche, M., Lattante, S., Kabashi, E., Jornea, L., Hannequin, D., & Brice, A. (2014). hnRNPA2B1 and hnRNPA1 mutations are rare in patients with “multisystem proteinopathy” and frontotemporal lobar degeneration phenotypes. Neurobiology of Aging. https://doi.org/10.1016/j.neurobiolaging.2013.09.016
Source records
- crossref · retrieved 2026-09-27T01:12:35.292Z