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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”

Detalles Bibliográficos
Autor principal: Graves, Tracey D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
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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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
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