This Danish startup intends to use a chaperone protein to treat lysosomal storage disorders.
This is a preview of subscription content, access via your institution
Access options
Subscribe to this journal
Receive 12 print issues and online access
$259.00 per year
only $21.58 per issue
Buy this article
- Purchase on SpringerLink
- Instant access to the full article PDF.
USD 39.95
Prices may be subject to local taxes which are calculated during checkout
Change history
04 June 2013
In the version of this article initially published, Steven Walkley's name was misspelled as Steven Walkely. The error has been corrected in the HTML and PDF versions of the article.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Garber, K. Orphazyme. Nat Biotechnol 31, 189 (2013). https://doi.org/10.1038/nbt0313-189
Published:
Issue date:
DOI: https://doi.org/10.1038/nbt0313-189
This article is cited by
-
Expanding rare disease drug trials based on shared molecular etiology
Nature Biotechnology (2014)
-
Erratum: Corrigendum: Editors' Pick: Orphazyme
Nature Biotechnology (2013)