Mitochondrial abnormalities in oculopharyngeal muscular dystrophy
This report describes a 56-yr-old man with a dominantly inherited disorder affecting four generations and characterized by bilateral ptosis and dysphagia. Muscle biopsy showed only minor light microscopic abnormalities but electron microscopy revealed fibres containing paracrystalline mitochondrial...
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Format: | Article |
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Faculty of Medicine, University of Malaya
1996
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Online Access: | http://eprints.um.edu.my/24487/ https://jummec.um.edu.my/issue/view/661/Vol.1%2C%20No.2%2C%201996 |
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