Title

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

Document Type

Other

Publisher

Frontiers Media

School

School of Medical and Health Sciences

Comments

Originally published as:

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. Advance Online Publication.

Original article available here.

DOI

10.3389/fnins.2018.00570

Access Rights

Free_to_read

Creative Commons License

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

Share

 
COinS