Correction to: A Germany-wide survey study on the patient journey of patients with hereditary angioedema
- DOI
- 10.1186/s13023-021-01714-7
- Published
- 2021-02-22
- Container
- Orphanet Journal of Rare Diseases
- Publisher
- Springer Science and Business Media LLC
- 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:10.1186/s13023-021-01714-7,
title = {Correction to: A Germany-wide survey study on the patient journey of patients with hereditary angioedema},
author = {Markus Magerl and Holger Gothe and Simon Krupka and Anja Lachmann and Christoph Ohlmeier},
year = {2021},
journal = {Orphanet Journal of Rare Diseases},
doi = {10.1186/s13023-021-01714-7},
url = {https://doi.org/10.1186/s13023-021-01714-7}
}RIS
TY - JOUR TI - Correction to: A Germany-wide survey study on the patient journey of patients with hereditary angioedema AU - Markus Magerl AU - Holger Gothe AU - Simon Krupka AU - Anja Lachmann AU - Christoph Ohlmeier PY - 2021 JO - Orphanet Journal of Rare Diseases DO - 10.1186/s13023-021-01714-7 UR - https://doi.org/10.1186/s13023-021-01714-7 ER -
APA
Magerl, M., Gothe, H., Krupka, S., Lachmann, A., & Ohlmeier, C. (2021). Correction to: A Germany-wide survey study on the patient journey of patients with hereditary angioedema. Orphanet Journal of Rare Diseases. https://doi.org/10.1186/s13023-021-01714-7
Source records
- crossref · retrieved 2026-09-26T06:28:56.606Z