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

Bibliographic Details
Main Authors:	Yan Lu, Yu-Wei Da, Yong-Biao Zhang, Xin-Gang Li, Min Wang, Li Di, Mi Pang, Lin Lei
Format:	Article
Language:	English
Published:	Frontiers Media S.A. 2018-08-01
Series:	Frontiers in Neuroscience
Subjects:	hereditary inclusion body myopathy next-generation sequencing CFTR mutation whole-exome sequencing
Online Access:	https://www.frontiersin.org/article/10.3389/fnins.2018.00570/full

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