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...

Description complète

Enregistré dans:
Détails bibliographiques
Publié dans:Skelet Muscle
Auteurs principaux: Mata López, Sara, Hammond, James J., Rigsby, Madison B., Balog-Alvarez, Cynthia J., Kornegay, Joe N., Nghiem, Peter P.
Format: Artigo
Langue:Inglês
Publié: BioMed Central 2018
Sujets:
Case Report
Accès en ligne: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
Tags: Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!

Documents similaires