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pubmed-article:19758981pubmed:abstractTextLipid-storage myopathy (LSM), defined by triglyceride accumulation in muscle fibres, is a heterogeneous group of lipid metabolic disorders predominantly affecting skeletal muscle. In the past 15 years, more than 200 cases of LSM have been reported in the Chinese literature, but the accurate pathogenic mechanisms are still unknown.lld:pubmed
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pubmed-article:19758981pubmed:articleTitleRiboflavin-responsive lipid-storage myopathy caused by ETFDH gene mutations.lld:pubmed
pubmed-article:19758981pubmed:affiliationLaboratory of Neuromuscular Disorders and Department of Neurology, Qilu Hospital, Shandong University, Jinan, PR China.lld:pubmed
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