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Peripheral neuropathy in myotonic dystrophy type 1

✍ Scribed by Mieke C. E. Hermans; Catharina G. Faber; Els K. Vanhoutte; Mayienne Bakkers; Marc H. De Baets; Christine E. M. de Die-Smulders; Ingemar S. J. Merkies

Book ID
109116377
Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
460 KB
Volume
16
Category
Article
ISSN
1085-9489

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Therapeutics development in myotonic dys
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✍ Erin Pennock Foff; Mani S. Mahadevan πŸ“‚ Article πŸ“… 2011 πŸ› John Wiley and Sons 🌐 English βš– 238 KB

## 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