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...

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Detalles Bibliográficos
Autores principales: Zhou, Jiapeng, Xin, Jing, Niu, Yayun, Wu, Shiwen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Software
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

Internet

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

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