Plasma lipidomic analysis shows a disease progression signature in mdx mice

Abstract Duchenne muscular dystrophy (DMD) is a rare genetic disorder affecting paediatric patients. The disease course is characterized by loss of muscle mass, which is rapidly substituted by fibrotic and adipose tissue. Clinical and preclinical models have clarified the processes leading to muscle...

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Bibliographic Details
Main Authors: Roula Tsonaka, Alexandre Seyer, Annemieke Aartsma-Rus, Pietro Spitali
Format: Article
Language:English
Published: Nature Publishing Group 2021-06-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-92406-6