An error was found in the first and second sentence of the original article's abstract.
It had originally been published as:
Hereditary inclusion body myopathy (HIBM) is a rare autosomal recessive adult onset muscle disease which affects one to three individuals per million worldwide. This disease is autosomal dominant and occurs in adulthood.
The corrected sentences should read:
Hereditary Inclusion Body Myopathy (HIBM) is a rare autosomal dominant or recessive adult onset muscle disease which affects one to three individuals per million worldwide. This disease is autosomal dominant or recessive and occurs in adulthood.
The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way.
The original article has been updated.
Statements
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Summary
Keywords
hereditary inclusion body myopathy, next-generation sequencing, CFTR, mutation, whole-exome sequencing
Citation
Lu Y, Da Y-W, Zhang Y-B, Li X-G, Wang M, Di L, Pang M and Lei L (2018) Corrigendum: Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis. Front. Neurosci. 12:570. doi: 10.3389/fnins.2018.00570
Received
10 July 2018
Accepted
27 July 2018
Published
22 August 2018
Volume
12 - 2018
Edited and reviewed by
Hua Lou, Case Western Reserve University, United States
Updates
Copyright
© 2018 Lu, Da, Zhang, Li, Wang, Di, Pang and Lei.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Yu-Wei Da yuwei_da@163.comYong-Biao Zhang zhangyongbiao@gmail.com
This article was submitted to Neurogenomics, a section of the journal Frontiers in Neuroscience
Disclaimer
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.