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Q38949682-6EE8BDF2-C5CF-410D-8000-2FC29244D30A
Q38949682-6EE8BDF2-C5CF-410D-8000-2FC29244D30A
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http://www.wikidata.org/entity/statement/Q38949682-6EE8BDF2-C5CF-410D-8000-2FC29244D30A
Dutch myotonic dystrophy type 2 patients and a North-African DM2 family carry the common European founder haplotype.
P2860
Q38949682-6EE8BDF2-C5CF-410D-8000-2FC29244D30A
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http://www.wikidata.org/entity/statement/Q38949682-6EE8BDF2-C5CF-410D-8000-2FC29244D30A
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be7e6e99558dfb610f4a20be57d2af3029fb3114
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.