Oculopharyngeal Muscular Dystrophy

About the Disease
Oculopharyngeal Muscular Dystrophy, also known as muscular dystrophy, oculopharyngeal, is related to muscular dystrophy and myopathy, and has symptoms including facial paresis An important gene associated with Oculopharyngeal Muscular Dystrophy is PABPN1 (Poly(A) Binding Protein Nuclear 1), and among its related pathways/superpathways are Processing of Capped Intron-Containing Pre-mRNA and Translational Control. Affiliated tissues include eye, tongue and lung, and related phenotypes are ptosis and myopathy

Common Targets
HNRNPA2B1 | Chaperone (nonspecified subtype) | NRL | LRP12 | PABPN1

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