Orphanet Journal of Rare Diseases (Feb 2021)

Correction to: A Germany-wide survey study on the patient journey of patients with hereditary angioedema

  • Markus Magerl,
  • Holger Gothe,
  • Simon Krupka,
  • Anja Lachmann,
  • Christoph Ohlmeier

DOI
https://doi.org/10.1186/s13023-021-01714-7
Journal volume & issue
Vol. 16, no. 1
pp. 1 – 1

Abstract

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An amendment to this paper has been published and can be accessed via the original article.