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

Authors/Creators

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

Abstract

A Corrigendum on Identification of the CFTR c.1666A>G 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's abstract.

Document Type

Other

Date of Publication

2018

School

School of Medical and Health Sciences

Creative Commons License

This work is licensed under a Creative Commons Attribution 4.0 License.

Publisher

Frontiers Media

Comments

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. Frontiers in Neuroscience, 12, Article 570.

https://doi.org/10.3389/fnins.2018.00570

Recommended Citation

Lu, Y., Da, Y., Zhang, Y., Li, X., Wang, M., Di, L., Pang, M., & Lei, L. (2018). Corrigendum: Identification of the CFTR c.1666A > G mutation in hereditary inclusion body myopathy using next-generation sequencing analysis. DOI: https://doi.org/10.3389/fnins.2018.00570