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[The inherited causes are: i) metabolic with failure of energy production, including mitochondrial fatty acid �-oxidation defects, LPIN1 mutations, inborn errors of glycogenolysis and glycolysis, more rarely mitochondrial respiratory chain deficiency, purine defects and peroxysomal ?-methyl-acyl-CoA-racemase defect (AMACR), ii) structural causes with muscle dystrophies and myopathies, iii) calcium pump disorder with RYR1 gene mutations, iv) inflammatory causes with myositis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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