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Mitochondrial Myopathies:Clinical & Biochem Features of 30 Patients with Major Deletions of Muscle Mitochondrial DNA Ann Neurol 26:699-708, Hold,I.J.,et al, 1989 See this aricle in Pubmed Article Abstract No abstract available for this article

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(click to filter results - removes previous filter) familial genetic neurologic disorders Kearns-Sayre syndrome mitochondrial disease myopathy myopathy,mitochondrial ophthalmoplegia ophthalmoplegia,progressive external retinopathy weakness

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