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Q39333700-B4F4F6FA-5779-48F7-B1F1-17AC19C75332
Q39333700-B4F4F6FA-5779-48F7-B1F1-17AC19C75332
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http://www.wikidata.org/entity/statement/Q39333700-B4F4F6FA-5779-48F7-B1F1-17AC19C75332
Biomolecular diagnosis of myotonic dystrophy type 2: a challenging approach.
P2860
Q39333700-B4F4F6FA-5779-48F7-B1F1-17AC19C75332
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http://www.wikidata.org/entity/statement/Q39333700-B4F4F6FA-5779-48F7-B1F1-17AC19C75332
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099227257631e4ee9e0884d03e327f9c429914da
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.