Cargando…

A Novel Mutation in N-Terminal Actin-Binding Domain of the DMD Gene Presenting Becker Muscular Dystrophy as Recurrent Exertional Rhabdomyolysis: A Case Report

Detalles Bibliográficos
Autor principal: Lee, Jong-Mok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7001431/
https://www.ncbi.nlm.nih.gov/pubmed/32055135
http://dx.doi.org/10.4103/aian.AIAN_215_19
_version_ 1783494243345498112
author Lee, Jong-Mok
author_facet Lee, Jong-Mok
author_sort Lee, Jong-Mok
collection PubMed
description
format Online
Article
Text
id pubmed-7001431
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Medknow Publications & Media Pvt Ltd
record_format MEDLINE/PubMed
spelling pubmed-70014312020-02-13 A Novel Mutation in N-Terminal Actin-Binding Domain of the DMD Gene Presenting Becker Muscular Dystrophy as Recurrent Exertional Rhabdomyolysis: A Case Report Lee, Jong-Mok Ann Indian Acad Neurol Letters to the Editor Medknow Publications & Media Pvt Ltd 2020 /pmc/articles/PMC7001431/ /pubmed/32055135 http://dx.doi.org/10.4103/aian.AIAN_215_19 Text en Copyright: © 2006-2020 Annals of Indian Academy of Neurology http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Letters to the Editor
Lee, Jong-Mok
A Novel Mutation in N-Terminal Actin-Binding Domain of the DMD Gene Presenting Becker Muscular Dystrophy as Recurrent Exertional Rhabdomyolysis: A Case Report
title A Novel Mutation in N-Terminal Actin-Binding Domain of the DMD Gene Presenting Becker Muscular Dystrophy as Recurrent Exertional Rhabdomyolysis: A Case Report
title_full A Novel Mutation in N-Terminal Actin-Binding Domain of the DMD Gene Presenting Becker Muscular Dystrophy as Recurrent Exertional Rhabdomyolysis: A Case Report
title_fullStr A Novel Mutation in N-Terminal Actin-Binding Domain of the DMD Gene Presenting Becker Muscular Dystrophy as Recurrent Exertional Rhabdomyolysis: A Case Report
title_full_unstemmed A Novel Mutation in N-Terminal Actin-Binding Domain of the DMD Gene Presenting Becker Muscular Dystrophy as Recurrent Exertional Rhabdomyolysis: A Case Report
title_short A Novel Mutation in N-Terminal Actin-Binding Domain of the DMD Gene Presenting Becker Muscular Dystrophy as Recurrent Exertional Rhabdomyolysis: A Case Report
title_sort novel mutation in n-terminal actin-binding domain of the dmd gene presenting becker muscular dystrophy as recurrent exertional rhabdomyolysis: a case report
topic Letters to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7001431/
https://www.ncbi.nlm.nih.gov/pubmed/32055135
http://dx.doi.org/10.4103/aian.AIAN_215_19
work_keys_str_mv AT leejongmok anovelmutationinnterminalactinbindingdomainofthedmdgenepresentingbeckermusculardystrophyasrecurrentexertionalrhabdomyolysisacasereport
AT leejongmok novelmutationinnterminalactinbindingdomainofthedmdgenepresentingbeckermusculardystrophyasrecurrentexertionalrhabdomyolysisacasereport