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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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Bibliografiske detaljer
Udgivet i: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
Sprog:Inglês
Udgivet: BioMed Central 2018
Fag:
Online adgang: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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