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Q47303392-9CEA914C-1A38-4230-8341-D9425403B3DC
Q47303392-9CEA914C-1A38-4230-8341-D9425403B3DC
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http://www.wikidata.org/entity/statement/Q47303392-9CEA914C-1A38-4230-8341-D9425403B3DC
Nuclear ribonucleoprotein-containing foci increase in size in non-dividing cells from patients with myotonic dystrophy type 2.
P2860
Q47303392-9CEA914C-1A38-4230-8341-D9425403B3DC
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Statement
http://www.wikidata.org/entity/statement/Q47303392-9CEA914C-1A38-4230-8341-D9425403B3DC
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482bf35cc42fa7f34c8026b61765fd6e137c89fa
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.