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Current Outline of Exon Skipping Trials in Duchenne Muscular Dystrophy
Molecular treatments for Duchenne muscular dystrophy (DMD) are already in clinical practice. One particular means is exon skipping, an approach which has more than 15 years of background. There are several promising clinical trials based on earlier works. The aim is to be able to initiate the produc...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9320322/ https://www.ncbi.nlm.nih.gov/pubmed/35886024 http://dx.doi.org/10.3390/genes13071241 |
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author | Eser, Gökçe Topaloğlu, Haluk |
author_facet | Eser, Gökçe Topaloğlu, Haluk |
author_sort | Eser, Gökçe |
collection | PubMed |
description | Molecular treatments for Duchenne muscular dystrophy (DMD) are already in clinical practice. One particular means is exon skipping, an approach which has more than 15 years of background. There are several promising clinical trials based on earlier works. The aim is to be able to initiate the production of enough dystrophin to change the rate of progression and create a clinical shift towards the better. Some of these molecules already have received at least conditional approval by health authorities; however, we still need new accumulating data. |
format | Online Article Text |
id | pubmed-9320322 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-93203222022-07-27 Current Outline of Exon Skipping Trials in Duchenne Muscular Dystrophy Eser, Gökçe Topaloğlu, Haluk Genes (Basel) Review Molecular treatments for Duchenne muscular dystrophy (DMD) are already in clinical practice. One particular means is exon skipping, an approach which has more than 15 years of background. There are several promising clinical trials based on earlier works. The aim is to be able to initiate the production of enough dystrophin to change the rate of progression and create a clinical shift towards the better. Some of these molecules already have received at least conditional approval by health authorities; however, we still need new accumulating data. MDPI 2022-07-14 /pmc/articles/PMC9320322/ /pubmed/35886024 http://dx.doi.org/10.3390/genes13071241 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Eser, Gökçe Topaloğlu, Haluk Current Outline of Exon Skipping Trials in Duchenne Muscular Dystrophy |
title | Current Outline of Exon Skipping Trials in Duchenne Muscular Dystrophy |
title_full | Current Outline of Exon Skipping Trials in Duchenne Muscular Dystrophy |
title_fullStr | Current Outline of Exon Skipping Trials in Duchenne Muscular Dystrophy |
title_full_unstemmed | Current Outline of Exon Skipping Trials in Duchenne Muscular Dystrophy |
title_short | Current Outline of Exon Skipping Trials in Duchenne Muscular Dystrophy |
title_sort | current outline of exon skipping trials in duchenne muscular dystrophy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9320322/ https://www.ncbi.nlm.nih.gov/pubmed/35886024 http://dx.doi.org/10.3390/genes13071241 |
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