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The Status of Exon Skipping as a Therapeutic Approach to Duchenne Muscular Dystrophy

Duchenne muscular dystrophy (DMD) is associated with mutations in the dystrophin gene that disrupt the open reading frame whereas the milder Becker's form is associated with mutations which leave an in-frame mRNA transcript that can be translated into a protein that includes the N- and C- termi...

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Detalhes bibliográficos
Main Authors: Lu, Qi-Long, Yokota, Toshifumi, Takeda, Shin'ichi, Garcia, Luis, Muntoni, Francesco, Partridge, Terence
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2011
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3017449/
https://ncbi.nlm.nih.gov/pubmed/20978473
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/mt.2010.219
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