Journal
Orphanet Journal of Rare Diseases
Publication Date
5-26-2020
Volume
15
Issue
1
First Page
126
Document Type
Open Access Publication
DOI
10.1186/s13023-020-01379-8
Rights and Permissions
Opladen, T., López-Laso, E., Cortès-Saladelafont, E. et al. Consensus guideline for the diagnosis and treatment of tetrahydrobiopterin (BH4) deficiencies. Orphanet J Rare Dis 15, 126 (2020). https://doi.org/10.1186/s13023-020-01379-8 This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
Recommended Citation
Opladen, Thomas; Pearson, Toni S; and et al, "Consensus guideline for the diagnosis and treatment of tetrahydrobiopterin (BH4) deficiencies." Orphanet Journal of Rare Diseases. 15, 1. 126 (2020).
https://digitalcommons.wustl.edu/open_access_pubs/9903
Table S1. Key questions for the Guideline on diagnosis and treatment of BH4 deficiencies.
13023_2020_1379_MOESM2_ESM.tif (69 kB)
Figure S2. Flow chart showing the systematic literature search, and number and type of included sources.
s13023-020-01464-y.pdf (885 kB)
Correction to: Orphanet Journal of Rare Diseases 15, 126 (2020)