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Novel Mutations in SCN4A Gene Cause Myotonia Congenita with Scoliosis

Detalles Bibliográficos
Autores principales: Xu, Yang-Qi, Liu, Xiao-Li, Huang, Xiao-Jun, Tian, Wo-Tu, Tang, Hui-Dong, Cao, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5830834/
https://www.ncbi.nlm.nih.gov/pubmed/29451154
http://dx.doi.org/10.4103/0366-6999.225061
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author Xu, Yang-Qi
Liu, Xiao-Li
Huang, Xiao-Jun
Tian, Wo-Tu
Tang, Hui-Dong
Cao, Li
author_facet Xu, Yang-Qi
Liu, Xiao-Li
Huang, Xiao-Jun
Tian, Wo-Tu
Tang, Hui-Dong
Cao, Li
author_sort Xu, Yang-Qi
collection PubMed
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spelling pubmed-58308342018-03-07 Novel Mutations in SCN4A Gene Cause Myotonia Congenita with Scoliosis Xu, Yang-Qi Liu, Xiao-Li Huang, Xiao-Jun Tian, Wo-Tu Tang, Hui-Dong Cao, Li Chin Med J (Engl) Clinical Observation Medknow Publications & Media Pvt Ltd 2018-02-20 /pmc/articles/PMC5830834/ /pubmed/29451154 http://dx.doi.org/10.4103/0366-6999.225061 Text en Copyright: © 2018 Chinese Medical Journal http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Clinical Observation
Xu, Yang-Qi
Liu, Xiao-Li
Huang, Xiao-Jun
Tian, Wo-Tu
Tang, Hui-Dong
Cao, Li
Novel Mutations in SCN4A Gene Cause Myotonia Congenita with Scoliosis
title Novel Mutations in SCN4A Gene Cause Myotonia Congenita with Scoliosis
title_full Novel Mutations in SCN4A Gene Cause Myotonia Congenita with Scoliosis
title_fullStr Novel Mutations in SCN4A Gene Cause Myotonia Congenita with Scoliosis
title_full_unstemmed Novel Mutations in SCN4A Gene Cause Myotonia Congenita with Scoliosis
title_short Novel Mutations in SCN4A Gene Cause Myotonia Congenita with Scoliosis
title_sort novel mutations in scn4a gene cause myotonia congenita with scoliosis
topic Clinical Observation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5830834/
https://www.ncbi.nlm.nih.gov/pubmed/29451154
http://dx.doi.org/10.4103/0366-6999.225061
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