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https://doi.org/10.1136/jmg.2005.037598
Copy DOIJournal: Journal of Medical Genetics | Publication Date: Apr 28, 2006 |
Citations: 32 |
Background: Oculopharyngeal muscular dystrophy (OPMD) is an autosomal dominant late onset neuromuscular disease characterised by proximal muscle weakness, ptosis, and swallowing difficulty. The only causative mutation described to date is...
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