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Limb-girdle muscular dystrophy 1F is caused by a microdeletion in the transportin 3 gene

Detalles Bibliográficos
Autor principal: Ortolano, Saida
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4652553/
http://dx.doi.org/10.1186/1750-1172-10-S2-O20
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author Ortolano, Saida
author_facet Ortolano, Saida
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spelling pubmed-46525532015-11-25 Limb-girdle muscular dystrophy 1F is caused by a microdeletion in the transportin 3 gene Ortolano, Saida Orphanet J Rare Dis Oral Presentation BioMed Central 2015-11-11 /pmc/articles/PMC4652553/ http://dx.doi.org/10.1186/1750-1172-10-S2-O20 Text en Copyright © 2015 Ortolano http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Oral Presentation
Ortolano, Saida
Limb-girdle muscular dystrophy 1F is caused by a microdeletion in the transportin 3 gene
title Limb-girdle muscular dystrophy 1F is caused by a microdeletion in the transportin 3 gene
title_full Limb-girdle muscular dystrophy 1F is caused by a microdeletion in the transportin 3 gene
title_fullStr Limb-girdle muscular dystrophy 1F is caused by a microdeletion in the transportin 3 gene
title_full_unstemmed Limb-girdle muscular dystrophy 1F is caused by a microdeletion in the transportin 3 gene
title_short Limb-girdle muscular dystrophy 1F is caused by a microdeletion in the transportin 3 gene
title_sort limb-girdle muscular dystrophy 1f is caused by a microdeletion in the transportin 3 gene
topic Oral Presentation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4652553/
http://dx.doi.org/10.1186/1750-1172-10-S2-O20
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