Corrigendum: Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis
- Resource Type
- article
- Source
- Frontiers in Neuroscience, Vol 12 (2018)
- Subject
hereditary inclusion body myopathy next-generation sequencing CFTR mutation whole-exome sequencing Neurosciences. Biological psychiatry. Neuropsychiatry RC321-571 - Language
- English
- ISSN
- 1662-453X