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Response to the paper titled “Identification of a novel CACNA1A mutation in a Chinese family with autosomal recessive progressive myoclonic epilepsy”
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6141117/ https://www.ncbi.nlm.nih.gov/pubmed/30254444 http://dx.doi.org/10.2147/NDT.S179068 |
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author | Graves, Tracey D |
author_facet | Graves, Tracey D |
author_sort | Graves, Tracey D |
collection | PubMed |
description | |
format | Online Article Text |
id | pubmed-6141117 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61411172018-09-25 Response to the paper titled “Identification of a novel CACNA1A mutation in a Chinese family with autosomal recessive progressive myoclonic epilepsy” Graves, Tracey D Neuropsychiatr Dis Treat Letter Dove Medical Press 2018-09-11 /pmc/articles/PMC6141117/ /pubmed/30254444 http://dx.doi.org/10.2147/NDT.S179068 Text en © 2018 Graves. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Letter Graves, Tracey D Response to the paper titled “Identification of a novel CACNA1A mutation in a Chinese family with autosomal recessive progressive myoclonic epilepsy” |
title | Response to the paper titled “Identification of a novel CACNA1A mutation in a Chinese family with autosomal recessive progressive myoclonic epilepsy” |
title_full | Response to the paper titled “Identification of a novel CACNA1A mutation in a Chinese family with autosomal recessive progressive myoclonic epilepsy” |
title_fullStr | Response to the paper titled “Identification of a novel CACNA1A mutation in a Chinese family with autosomal recessive progressive myoclonic epilepsy” |
title_full_unstemmed | Response to the paper titled “Identification of a novel CACNA1A mutation in a Chinese family with autosomal recessive progressive myoclonic epilepsy” |
title_short | Response to the paper titled “Identification of a novel CACNA1A mutation in a Chinese family with autosomal recessive progressive myoclonic epilepsy” |
title_sort | response to the paper titled “identification of a novel cacna1a mutation in a chinese family with autosomal recessive progressive myoclonic epilepsy” |
topic | Letter |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6141117/ https://www.ncbi.nlm.nih.gov/pubmed/30254444 http://dx.doi.org/10.2147/NDT.S179068 |
work_keys_str_mv | AT gravestraceyd responsetothepapertitledidentificationofanovelcacna1amutationinachinesefamilywithautosomalrecessiveprogressivemyoclonicepilepsy |