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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author Lu, Yan
Da, Yu-Wei
Zhang, Yong-Biao
Li, Xin-Gang
Wang, Min
Di, Li
Pang, Mi
Lei, Lin
author_facet Lu, Yan
Da, Yu-Wei
Zhang, Yong-Biao
Li, Xin-Gang
Wang, Min
Di, Li
Pang, Mi
Lei, Lin
author_sort Lu, Yan
collection PubMed
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spelling pubmed-61139272018-08-31 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 Front Neurosci Neuroscience Frontiers Media S.A. 2018-08-22 /pmc/articles/PMC6113927/ /pubmed/30174583 http://dx.doi.org/10.3389/fnins.2018.00570 Text en Copyright © 2018 Lu, Da, Zhang, Li, Wang, Di, Pang and Lei. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Lu, Yan
Da, Yu-Wei
Zhang, Yong-Biao
Li, Xin-Gang
Wang, Min
Di, Li
Pang, Mi
Lei, Lin
Corrigendum: Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis
title Corrigendum: Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis
title_full Corrigendum: Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis
title_fullStr Corrigendum: Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis
title_full_unstemmed Corrigendum: Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis
title_short Corrigendum: Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis
title_sort corrigendum: identification of the cftr c.1666a>g mutation in hereditary inclusion body myopathy using next-generation sequencing analysis
topic Neuroscience
url 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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