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LGMD phenotype due to a new gene and dysferlinopathy investigated by next-generation sequencing

Detalles Bibliográficos
Autor principal: Angelini, Corrado I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4811386/
https://www.ncbi.nlm.nih.gov/pubmed/27066575
http://dx.doi.org/10.1212/NXG.0000000000000039
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author Angelini, Corrado I.
author_facet Angelini, Corrado I.
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spelling pubmed-48113862016-04-08 LGMD phenotype due to a new gene and dysferlinopathy investigated by next-generation sequencing Angelini, Corrado I. Neurol Genet Editorial Wolters Kluwer 2015-12-10 /pmc/articles/PMC4811386/ /pubmed/27066575 http://dx.doi.org/10.1212/NXG.0000000000000039 Text en © 2015 American Academy of Neurology This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially.
spellingShingle Editorial
Angelini, Corrado I.
LGMD phenotype due to a new gene and dysferlinopathy investigated by next-generation sequencing
title LGMD phenotype due to a new gene and dysferlinopathy investigated by next-generation sequencing
title_full LGMD phenotype due to a new gene and dysferlinopathy investigated by next-generation sequencing
title_fullStr LGMD phenotype due to a new gene and dysferlinopathy investigated by next-generation sequencing
title_full_unstemmed LGMD phenotype due to a new gene and dysferlinopathy investigated by next-generation sequencing
title_short LGMD phenotype due to a new gene and dysferlinopathy investigated by next-generation sequencing
title_sort lgmd phenotype due to a new gene and dysferlinopathy investigated by next-generation sequencing
topic Editorial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4811386/
https://www.ncbi.nlm.nih.gov/pubmed/27066575
http://dx.doi.org/10.1212/NXG.0000000000000039
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