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Q37619968-631C8B35-5418-4D4F-985A-6E1D2AEAFBA7
Q37619968-631C8B35-5418-4D4F-985A-6E1D2AEAFBA7
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http://www.wikidata.org/entity/statement/Q37619968-631C8B35-5418-4D4F-985A-6E1D2AEAFBA7
Most expression and splicing changes in myotonic dystrophy type 1 and type 2 skeletal muscle are shared with other muscular dystrophies.
P2860
Q37619968-631C8B35-5418-4D4F-985A-6E1D2AEAFBA7
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http://www.wikidata.org/entity/statement/Q37619968-631C8B35-5418-4D4F-985A-6E1D2AEAFBA7
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wasDerivedFrom
36fa6e8ed43ef3bb50cf237891f46946be145287
P2860
Confirmation of the type 2 myotonic dystrophy (CCTG)n expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins: a single shared haplotype indicates an ancestral founder effect.