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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Bibliographic Details
Published in:Skelet Muscle
Main Authors: Mata López, Sara, Hammond, James J., Rigsby, Madison B., Balog-Alvarez, Cynthia J., Kornegay, Joe N., Nghiem, Peter P.
Format: Artigo
Language:Inglês
Published: BioMed Central 2018
Subjects:
Case Report
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC5975675/
https://ncbi.nlm.nih.gov/pubmed/29843823
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13395-018-0162-1
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