Corrigendum: Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis - Lu, Yan; Da, Yu-Wei; Zhang, Yong-Biao; Li, Xin-Gang; Wang, Min; Di, Li; Pang, Mi; Lei, Lin (Frontiers in Neuroscience, 2018)