A novel canine model for Duchenne muscular dystrophy (DMD): single nucleotide deletion in DMD gene exon 20

BACKGROUND: Boys with Duchenne muscular dystrophy (DMD) have DMD gene mutations, with associated loss of the dystrophin protein and progressive muscle degeneration and weakness. Corticosteroids and palliative support are currently the best treatment options. The long-term benefits of recently approv...

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Detalles Bibliográficos
Autores principales: Mata López, Sara, Hammond, James J., Rigsby, Madison B., Balog-Alvarez, Cynthia J., Kornegay, Joe N., Nghiem, Peter P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5975675/
https://www.ncbi.nlm.nih.gov/pubmed/29843823
http://dx.doi.org/10.1186/s13395-018-0162-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5975675/
https://www.ncbi.nlm.nih.gov/pubmed/29843823
http://dx.doi.org/10.1186/s13395-018-0162-1

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