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Author Zilbovicius M |
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Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Jacquette A ; Lemaitre H ; Angeard N ; Eymard B ; Whalen S ; Desguerre I ; Brunelle F ; Zilbovicius M ; Heron D ; Boddaert N | AFM-TELETHON | 2011Myotonic dystrophy type 1 (DM1) is an autosomal dominant inherited neuromuscular condition caused by an abnormal CTG triplet expansion within the 3' untranslated region of the myotonic dystrophy protein kinase (DMPK) gene on chromosome 19q35The [...]