The discovery of the DNA methylation episignature for Duchenne muscular dystrophy
Author:
Funder
Muscular Dystrophy Canada
Western University
Publisher
Elsevier BV
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
Reference75 articles.
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4. Absence of dystrophin disrupts skeletal muscle signaling: roles of Ca2+, reactive oxygen species, and nitric oxide in the development of muscular dystrophy;Allen;Physiol Rev,2016
5. Epigenetic modifications in muscle regeneration and progression of Duchenne muscular dystrophy;Rugowska;Clin Epigenetics,2021
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3. How Can Proteomics Help to Elucidate the Pathophysiological Crosstalk in Muscular Dystrophy and Associated Multi-System Dysfunction?;Proteomes;2024-01-16
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