Skip to main content

Advertisement

Correction to: Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease

Article metrics

The original article was published in Orphanet Journal of Rare Diseases 2018 13:155

Correction to: Orphanet J Rare Dis (2018) 13:155.

https://doi.org/10.1186/s13023-018-0889-0

The original version of this article [1] unfortunately included an error to an author’s name. Author Jordi Díaz-Manera was erroneously presented as Jorge Alberto Diaz Manera. The correct author name has been included in the author list of this Correction article.

For citation purposes the author’s given name is Jordi and family name Díaz-Manera. Therefore, the correct citation of the author’s details is: Díaz-Manera J.

Reference

  1. 1.

    Wood L, et al. Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease. Orphanet J Rare Dis. 2018;13(155). https://doi.org/10.1186/s13023-018-0889-0.

Download references

Author information

Correspondence to Libby Wood.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Wood, L., Bassez, G., Bleyenheuft, C. et al. Correction to: Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease. Orphanet J Rare Dis 14, 199 (2019) doi:10.1186/s13023-019-1157-7

Download citation