Corrigendum: Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis.

Yan Lu,Mi Pang,Lin Lei,Xin-Gang Li,Min Wang,Yong-Biao Zhang,Yu-Wei Da,Li Di

doi:10.3389/fnins.2018.00570

Abstract

[This corrects the article DOI: 10.3389/fnins.2018.00329.].

Highlights

Specialty section: This article was submitted to Neurogenomics, a section of the journal Frontiers in Neuroscience
The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way
Conflict of Interest Statement: 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

Introduction

Specialty section: This article was submitted to Neurogenomics, a section of the journal Frontiers in Neuroscience. Corrigendum: Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis Yan Lu 1, Yu-Wei Da 1*, Yong-Biao Zhang 2*, Xin-Gang Li 3,4, Min Wang 1, Li Di 1, Mi Pang 5 and Lin Lei 1

Results

Conclusion