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Read-through approach for stop mutations in Duchenne muscular dystrophy. An update

Dystrophinopathies are allelic conditions caused by deletions, duplications and point-mutations in the DMD gene, located on the X chromosome (Xp21.2). Mutations that prematurely interrupt the dystrophin protein synthesis lead to the most severe clinical form, Duchenne muscular Dystrophy, characteriz...

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Detalles Bibliográficos
Autor principal: Politano, Luisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pacini Editore Srl 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8033424/
https://www.ncbi.nlm.nih.gov/pubmed/33870095
http://dx.doi.org/10.36185/2532-1900-041

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