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

Detalles Bibliográficos
Autores principales:	Lu, Yan, Da, Yu-Wei, Zhang, Yong-Biao, Li, Xin-Gang, Wang, Min, Di, Li, Pang, Mi, Lei, Lin
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2018
Materias:	Neuroscience
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6113927/ https://www.ncbi.nlm.nih.gov/pubmed/30174583 http://dx.doi.org/10.3389/fnins.2018.00570

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