Da, Yu-Wei

Di, Li

Lei, Lin

Li, Xin-Gang

Lu, Yan

Pang, Mi

Wang, Min

Zhang, Yong-Biao

English

A Corrigendum on Identification of the CFTR c.1666A\u3eG Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis
by Lu, Y., Da, Y.-W., Zhang, Y.-B., Li, X.-G., Wang, M., Di, L., et al. (2018). Front. Neurosci. 12:329. doi: 10.3389/fnins.2018.00329
An error was found in the first and second sentence of the original article\u27s abstract

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Edith Cowan University Research Online ECU Publications Post 2013 2018 Corrigendum: Identification of the CFTR c.1666A > G mutation in hereditary inclusion body myopathy using next-generation sequencing analysis [Front. Neurosci., 12, (2018), (329)] doi: 10.3389/fnins.2018.00329 Yan Lu Yu-Wei Da Yong-Biao Zhang Xin-Gang Li Edith Cowan University, xingang.li@ecu.edu.au Min Wang See next page for additional authors Follow this and additional works at: https://ro.ecu.edu.au/ecuworkspost2013  Part of the Neurosciences Commons 10.3389/fnins.2018.00570 Lu, Y., Da, Y. W., Zhang, Y. B., Li, X. G., Wang, M., Di, L., ... & 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, (2018), (329)] doi: 10.3389/fnins.2018.00329. Frontiers in Neuroscience. Available here. This Other is posted at Research Online. https://ro.ecu.edu.au/ecuworkspost2013/5385 Authors Yan Lu, Yu-Wei Da, Yong-Biao Zhang, Xin-Gang Li, Min Wang, Li Di, Mi Pang, and Lin Lei This other is available at Research Online: https://ro.ecu.edu.au/ecuworkspost2013/5385 CORRECTIONpublished: 22 August 2018doi: 10.3389/fnins.2018.00570Frontiers in Neuroscience | www.frontiersin.org 1 August 2018 | Volume 12 | Article 570Edited and reviewed by:Hua Lou,Case Western Reserve University,United States*Correspondence:Yu-Wei Dayuwei_da@163.comYong-Biao Zhangzhangyongbiao@gmail.comSpecialty section:This article was submitted toNeurogenomics,a section of the journalFrontiers in NeuroscienceReceived: 10 July 2018Accepted: 27 July 2018Published: 22 August 2018Citation:Lu Y, Da Y-W, Zhang Y-B, Li X-G,Wang M, Di L, Pang M and Lei L(2018) Corrigendum: Identification ofthe CFTR c.1666A>G Mutation inHereditary Inclusion Body MyopathyUsing Next-Generation SequencingAnalysis. Front. Neurosci. 12:570.doi: 10.3389/fnins.2018.00570Corrigendum: Identification of theCFTR c.1666A>G Mutation inHereditary Inclusion Body MyopathyUsing Next-Generation SequencingAnalysisYan Lu 1, Yu-Wei Da 1*, Yong-Biao Zhang 2*, Xin-Gang Li 3,4, Min Wang 1, Li Di 1, Mi Pang 5and Lin Lei 11Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China, 2Beijing Advanced Innovation Centerfor Big Data-Based Precision Medicine, Beihang University, Beijing, China, 3 Beijing Institute of Genomics, Chinese Academyof Sciences, Beijing, China, 4 School of Medical and Health Sciences, Edith Cowan University, Joondalup, WA, Australia,5Department of Neurology, Zhengzhou University People’s Hospital, Zhengzhou, ChinaKeywords: hereditary inclusion body myopathy, next-generation sequencing, CFTR, mutation, whole-exomesequencingA Corrigendum onIdentification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body MyopathyUsing Next-Generation Sequencing Analysisby Lu, Y., Da, Y.-W., Zhang, Y.-B., Li, X.-G., Wang, M., Di, L., et al. (2018). Front. Neurosci. 12:329.doi: 10.3389/fnins.2018.00329An 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 muscledisease which affects one to three individuals per million worldwide. This disease is autosomaldominant and occurs in adulthood.The corrected sentences should read:Hereditary Inclusion Body Myopathy (HIBM) is a rare autosomal dominant or recessive adultonset muscle disease which affects one to three individuals per million worldwide. This disease isautosomal dominant or recessive and occurs in adulthood.The authors apologize for this error and state that this does not change the scientific conclusionsof the article in any way.The original article has been updated.Conflict of Interest Statement: The authors declare that the research was conducted in the absence of any commercial orfinancial relationships that could be construed as a potential conflict of interest.Copyright © 2018 Lu, Da, Zhang, Li, Wang, Di, Pang and Lei. This is an open-access article distributed under the terms of theCreative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided theoriginal author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordancewith accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

Corrigendum: Identification of the CFTR c.1666A \u3e G mutation in hereditary inclusion body myopathy using next-generation sequencing analysis

https://ro.ecu.edu.au/cgi/viewcontent.cgi?article=6392&amp;context=ecuworkspost2013

Corrigendum: Identification of the CFTR c.1666A \u3e G mutation in hereditary inclusion body myopathy using next-generation sequencing analysis [Front. Neurosci., 12, (2018), (329)] doi: 10.3389/fnins.2018.00329

Corrigendum: Identification of the CFTR c.1666A \u3e G mutation in hereditary inclusion body myopathy using next-generation sequencing analysis [Front. Neurosci., 12, (2018), (329)] doi: 10.3389/fnins.2018.00329

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