Multiomic characterization of disease progression in mice lacking dystrophin

Duchenne muscular dystrophy (DMD) is caused by genetic mutations leading to lack of dystrophin in skeletal muscle. A better understanding of how objective biomarkers for DMD vary across subjects and over time is needed to model disease progression and response to therapy more effectively, both in pr...

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Detalles Bibliográficos
Autores principales: Signorelli, Mirko, Tsonaka, Roula, Aartsma-Rus, Annemieke, Spitali, Pietro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10065259/
https://www.ncbi.nlm.nih.gov/pubmed/37000843
http://dx.doi.org/10.1371/journal.pone.0283869

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10065259/
https://www.ncbi.nlm.nih.gov/pubmed/37000843
http://dx.doi.org/10.1371/journal.pone.0283869

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