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Q33836050-EA4F1F3F-B1D3-4EBB-BC2C-44250CECB730
Q33836050-EA4F1F3F-B1D3-4EBB-BC2C-44250CECB730
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http://www.wikidata.org/entity/statement/Q33836050-EA4F1F3F-B1D3-4EBB-BC2C-44250CECB730
High frequency of co-segregating CLCN1 mutations among myotonic dystrophy type 2 patients from Finland and Germany.
P2860
Q33836050-EA4F1F3F-B1D3-4EBB-BC2C-44250CECB730
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Statement
http://www.wikidata.org/entity/statement/Q33836050-EA4F1F3F-B1D3-4EBB-BC2C-44250CECB730
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2629535e1fecda1aec6afd99ec3b4cb54f7aa8be
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.