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Electrocardiographic Abnormalities and Sudden Death in Myotonic Dystrophy Type 1

✍ Scribed by Groh, William J.; Groh, Miriam R.; Saha, Chandan; Kincaid, John C.; Simmons, Zachary; Ciafaloni, Emma; Pourmand, Rahman; Otten, Richard F.; Bhakta, Deepak; Nair, Girish V.; Marashdeh, Mohammad M.; Zipes, Douglas P.; Pascuzzi, Robert M.

Book ID: 126201126
Publisher: Massachusetts Medical Society
Year: 2008
Tongue: English
Weight: 161 KB
Volume: 358
Category: Article
ISSN: 0096-6762
DOI: 10.1056/NEJMoa062800

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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