Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia.
- DOI
- 10.1136/jnnp.2008.167528
- Published
- 2009 Dec
- Container
- Journal of neurology, neurosurgery, and psychiatry
- 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:10.1136/jnnp.2008.167528,
title = {Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia.},
author = {Schüle R and Schlipf N and Synofzik M and Klebe S and Klimpe S and Hehr U and Winner B and Lindig T and Dotzer A and Riess O and Winkler J and Schöls L and Bauer P},
year = {2009},
journal = {Journal of neurology, neurosurgery, and psychiatry},
doi = {10.1136/jnnp.2008.167528},
url = {https://doi.org/10.1136/jnnp.2008.167528}
}RIS
TY - JOUR TI - Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia. AU - Schüle R AU - Schlipf N AU - Synofzik M AU - Klebe S AU - Klimpe S AU - Hehr U AU - Winner B AU - Lindig T AU - Dotzer A AU - Riess O AU - Winkler J AU - Schöls L AU - Bauer P PY - 2009 JO - Journal of neurology, neurosurgery, and psychiatry DO - 10.1136/jnnp.2008.167528 UR - https://doi.org/10.1136/jnnp.2008.167528 ER -
APA
R, S., N, S., M, S., S, K., S, K., U, H., B, W., T, L., A, D., O, R., J, W., L, S., & P, B. (2009). Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia.. Journal of neurology, neurosurgery, and psychiatry. https://doi.org/10.1136/jnnp.2008.167528
Source records
- pubmed · retrieved 2026-09-25T23:30:34.056Z
- europe-pmc · retrieved 2026-09-25T23:30:34.075Z
- hal · retrieved 2026-09-25T23:30:34.128Z