Immortalized human myotonic dystrophy muscle cell lines to assess therapeutic compounds
Myotonic dystrophy type 1 (DM1) and type 2 (DM2) are autosomal dominant neuromuscular diseases caused by microsatellite expansions and belong to the family of RNA-dominant disorders. Availability of cellular models in which the DM mutation is expressed within its natural context is essential to faci...
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Main Authors: | , , , , , , , , , , , , , , , , , |
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Format: | Book |
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The Company of Biologists,
2017-04-01T00:00:00Z.
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Internet
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Call Number: |
A1234.567 |
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Copy 1 | Available |