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Q54982478-9C81C097-F648-401E-90A1-5EA4639C3809
Q54982478-9C81C097-F648-401E-90A1-5EA4639C3809
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54982478-9C81C097-F648-401E-90A1-5EA4639C3809
Abnormalities in Skeletal Muscle Myogenesis, Growth, and Regeneration in Myotonic Dystrophy.
P2860
Q54982478-9C81C097-F648-401E-90A1-5EA4639C3809
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54982478-9C81C097-F648-401E-90A1-5EA4639C3809
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Statement
wasDerivedFrom
c35b857f9af67d7e74cc3d8bfd1a93755251857a
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.