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The presence of such intranuclear structures should be added to the criteria of the clinical picture and the family history for diagnosis of a case and inclusion of a family in further genetic studies. Reverse genetic studies of large families and biochemical studies of these intranuclear structures may help to understand the pathogenesis of this common disease in Quebec.<\/jats:p>","DOI":"10.1017\/s0317167100029565","type":"journal-article","created":{"date-parts":[[2016,7,28]],"date-time":"2016-07-28T11:40:29Z","timestamp":1469706029000},"page":"446-450","source":"Crossref","is-referenced-by-count":29,"title":["Nuclear Inclusions in Oculopharyngeal Muscular Dystrophy in Quebec"],"prefix":"10.1017","volume":"16","author":[{"given":"Jean-Pierre","family":"Bouchard","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Fran\u00e7ois","family":"Gagn\u00e9","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Fernando M. 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