KH176 under development for rare mitochondrial disease: a first in man randomized controlled clinical trial in healthy male volunteers
- DOI
- 10.1186/s13023-017-0715-0
- Published
- 2017-10-16
- Container
- Orphanet Journal of Rare Diseases
- Publisher
- Springer Science and Business Media LLC
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1186/s13023-017-0715-0,
title = {KH176 under development for rare mitochondrial disease: a first in man randomized controlled clinical trial in healthy male volunteers},
author = {Saskia Koene and Edwin Spaans and Luc Van Bortel and Griet Van Lancker and Brant Delafontaine and Fabio Badilini and Julien Beyrath and Jan Smeitink},
year = {2017},
journal = {Orphanet Journal of Rare Diseases},
doi = {10.1186/s13023-017-0715-0},
url = {https://doi.org/10.1186/s13023-017-0715-0}
}RIS
TY - JOUR TI - KH176 under development for rare mitochondrial disease: a first in man randomized controlled clinical trial in healthy male volunteers AU - Saskia Koene AU - Edwin Spaans AU - Luc Van Bortel AU - Griet Van Lancker AU - Brant Delafontaine AU - Fabio Badilini AU - Julien Beyrath AU - Jan Smeitink PY - 2017 JO - Orphanet Journal of Rare Diseases DO - 10.1186/s13023-017-0715-0 UR - https://doi.org/10.1186/s13023-017-0715-0 ER -
APA
Koene, S., Spaans, E., Bortel, L. V., Lancker, G. V., Delafontaine, B., Badilini, F., Beyrath, J., & Smeitink, J. (2017). KH176 under development for rare mitochondrial disease: a first in man randomized controlled clinical trial in healthy male volunteers. Orphanet Journal of Rare Diseases. https://doi.org/10.1186/s13023-017-0715-0
Source records
- crossref · retrieved 2026-09-25T22:23:04.459Z