Compound Heterozygous COA7 Variants Presenting With Childhood-Onset Axonal Neuropathy in 2 Siblings.
- DOI
- 10.1212/nxg.0000000000200394
- Published
- 2026 Jun
- Container
- Neurology. Genetics
- 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:10.1212/nxg.0000000000200394,
title = {Compound Heterozygous COA7 Variants Presenting With Childhood-Onset Axonal Neuropathy in 2 Siblings.},
author = {Cicala G and Rolleri E and Berti B and Luigetti M and Forcina N and Villa M and Capasso A and Arpaia C and Malaspina M and Fattori F and Bosco L and Primiano G and Novelli A and Rizza T and Bertini E and Pane M and Mercuri E},
year = {2026},
journal = {Neurology. Genetics},
doi = {10.1212/nxg.0000000000200394},
url = {https://doi.org/10.1212/nxg.0000000000200394}
}RIS
TY - JOUR TI - Compound Heterozygous COA7 Variants Presenting With Childhood-Onset Axonal Neuropathy in 2 Siblings. AU - Cicala G AU - Rolleri E AU - Berti B AU - Luigetti M AU - Forcina N AU - Villa M AU - Capasso A AU - Arpaia C AU - Malaspina M AU - Fattori F AU - Bosco L AU - Primiano G AU - Novelli A AU - Rizza T AU - Bertini E AU - Pane M AU - Mercuri E PY - 2026 JO - Neurology. Genetics DO - 10.1212/nxg.0000000000200394 UR - https://doi.org/10.1212/nxg.0000000000200394 ER -
APA
G, C., E, R., B, B., M, L., N, F., M, V., A, C., C, A., M, M., F, F., L, B., G, P., A, N., T, R., E, B., M, P., & E, M. (2026). Compound Heterozygous COA7 Variants Presenting With Childhood-Onset Axonal Neuropathy in 2 Siblings.. Neurology. Genetics. https://doi.org/10.1212/nxg.0000000000200394
Source records
- pubmed · retrieved 2026-09-27T00:25:39.836Z