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DMDtoolkit: a tool for visualizing the mutated dystrophin protein and predicting the clinical severity in DMD
BACKGROUND: Dystrophinopathy is one of the most common human monogenic diseases which results in Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD). Mutations in the dystrophin gene are responsible for both DMD and BMD. However, the clinical phenotypes and treatments are quite dif...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2017
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5290630/ https://www.ncbi.nlm.nih.gov/pubmed/28152980 http://dx.doi.org/10.1186/s12859-017-1504-4 |