Open Access

Erratum to: Expression profiling of white sponge nevus by RNA sequencing revealed pathological pathways

Contributed equally
Orphanet Journal of Rare Diseases201510:119

https://doi.org/10.1186/s13023-015-0308-8

Received: 17 July 2015

Accepted: 17 July 2015

Published: 23 September 2015

The original article was published in Orphanet Journal of Rare Diseases 2015 10:72

Erratum

After publication of [1] the authors realised that the original publication had two descriptive errors when referring to diseases. “periodontal” was written rather than “mucous membrane” in the article on page 1, lines 12 and 25. “periodontal disease” was written rather than “mucous membrane hyperkeratosis” in the article on page 2, lines 72 and 73. The correct spelling of these is included in this erratum.

Notes

Declarations

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.

Authors’ Affiliations

(1)
Department of Stomatology, Huashan Hospital, Fudan University
(2)
Laboratory of Oral Biomedical Science and Translational Medicine, School of Stomatology, Tongji University
(3)
School of Life sciences and Technology, Tongji University
(4)
State Key Laboratory of Medical Genetics, Central South University
(5)
Department of Ophthalmology, Shanghai Tenth People’s Hospital, Tongji University School of Medicine

Reference

  1. Wenping C, Beizhan J, Tienan F, Jinfeng X, Jianhua Y, Zhenghu C, et al. Expression profiling of white sponge nevus by RNA sequencing revealed pathological pathways. Orphanet Journal of Rare Diseases. 2015;10:72.View ArticleGoogle Scholar

Copyright

© Cai et al. 2015

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