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Q42793424-C399A6D0-9017-4DCF-B1D7-401948B7856F
Q42793424-C399A6D0-9017-4DCF-B1D7-401948B7856F
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http://www.wikidata.org/entity/statement/Q42793424-C399A6D0-9017-4DCF-B1D7-401948B7856F
Altered MEF2 isoforms in myotonic dystrophy and other neuromuscular disorders.
P2860
Q42793424-C399A6D0-9017-4DCF-B1D7-401948B7856F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42793424-C399A6D0-9017-4DCF-B1D7-401948B7856F
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wasDerivedFrom
134cbc377be5c5b253fc1ad1a1a3ce77d3acc560
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.