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Health supervision and anticipatory guidance in adult myotonic dystrophy type 1

✍ Scribed by C. Gagnon; M.C. Chouinard; L. Laberge; S. Veillette; P. Bégin; R. Breton; S. Jean; D. Brisson; D. Gaudet; J. Mathieu


Book ID
116794708
Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
177 KB
Volume
20
Category
Article
ISSN
0960-8966

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## Abstract Myotonic dystrophy (DM1), the most common adult muscular dystrophy, is a multisystem, autosomal dominant genetic disorder caused by an expanded CTG repeat that leads to nuclear retention of a mutant RNA and subsequent RNA toxicity. Significant insights into the molecular mechanisms of R