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Q37680017-17160B58-F24D-4876-824C-EF9508970BB5
Q37680017-17160B58-F24D-4876-824C-EF9508970BB5
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http://www.wikidata.org/entity/statement/Q37680017-17160B58-F24D-4876-824C-EF9508970BB5
Clinical and genetic analysis of the first known Asian family with myotonic dystrophy type 2.
P2860
Q37680017-17160B58-F24D-4876-824C-EF9508970BB5
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http://www.wikidata.org/entity/statement/Q37680017-17160B58-F24D-4876-824C-EF9508970BB5
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1249af08db5481d1c55dea7d9048e675ff453445
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.