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Corrigendum: Myotonic Myopathy With Secondary Joint and Skeletal Anomalies From the c.2386C>G, p.L796V Mutation in SCN4A

Detalles Bibliográficos
Autores principales: Elia, Nathaniel, Nault, Trystan, McMillan, Hugh J., Graham, Gail E., Huang, Lijia, Cannon, Stephen C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7099287/
https://www.ncbi.nlm.nih.gov/pubmed/32265824
http://dx.doi.org/10.3389/fneur.2020.00181
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author Elia, Nathaniel
Nault, Trystan
McMillan, Hugh J.
Graham, Gail E.
Huang, Lijia
Cannon, Stephen C.
author_facet Elia, Nathaniel
Nault, Trystan
McMillan, Hugh J.
Graham, Gail E.
Huang, Lijia
Cannon, Stephen C.
author_sort Elia, Nathaniel
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spelling pubmed-70992872020-04-07 Corrigendum: Myotonic Myopathy With Secondary Joint and Skeletal Anomalies From the c.2386C>G, p.L796V Mutation in SCN4A Elia, Nathaniel Nault, Trystan McMillan, Hugh J. Graham, Gail E. Huang, Lijia Cannon, Stephen C. Front Neurol Neurology Frontiers Media S.A. 2020-03-20 /pmc/articles/PMC7099287/ /pubmed/32265824 http://dx.doi.org/10.3389/fneur.2020.00181 Text en Copyright © 2020 Elia, Nault, McMillan, Graham, Huang and Cannon. 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 Neurology
Elia, Nathaniel
Nault, Trystan
McMillan, Hugh J.
Graham, Gail E.
Huang, Lijia
Cannon, Stephen C.
Corrigendum: Myotonic Myopathy With Secondary Joint and Skeletal Anomalies From the c.2386C>G, p.L796V Mutation in SCN4A
title Corrigendum: Myotonic Myopathy With Secondary Joint and Skeletal Anomalies From the c.2386C>G, p.L796V Mutation in SCN4A
title_full Corrigendum: Myotonic Myopathy With Secondary Joint and Skeletal Anomalies From the c.2386C>G, p.L796V Mutation in SCN4A
title_fullStr Corrigendum: Myotonic Myopathy With Secondary Joint and Skeletal Anomalies From the c.2386C>G, p.L796V Mutation in SCN4A
title_full_unstemmed Corrigendum: Myotonic Myopathy With Secondary Joint and Skeletal Anomalies From the c.2386C>G, p.L796V Mutation in SCN4A
title_short Corrigendum: Myotonic Myopathy With Secondary Joint and Skeletal Anomalies From the c.2386C>G, p.L796V Mutation in SCN4A
title_sort corrigendum: myotonic myopathy with secondary joint and skeletal anomalies from the c.2386c>g, p.l796v mutation in scn4a
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7099287/
https://www.ncbi.nlm.nih.gov/pubmed/32265824
http://dx.doi.org/10.3389/fneur.2020.00181
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