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Browsing Research Articles (Neurology) by Subject "Oculopharyngeal muscular dystrophy (OPMD)"
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(Health and Medical Publishing Group, 2015-07)Autosomal dominantly inherited oculopharyngeal muscular dystrophy (OPMD) is caused by a trinucleotide repeat expansion in exon 1 of the polyadenylate binding protein nuclear 1 (PABPN1) gene on chromosome 14q. A large ...
Now showing items 1-1 of 1