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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Bibliographic Details
Main Authors: Wong, K.T., Dick, D., Anderson, J.E.R.
Format: Article
Published: 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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