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Q39081415-F4B5FE82-572F-45C0-AD9A-1CC0FDC18711
Q39081415-F4B5FE82-572F-45C0-AD9A-1CC0FDC18711
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http://www.wikidata.org/entity/statement/Q39081415-F4B5FE82-572F-45C0-AD9A-1CC0FDC18711
Myotonic dystrophy type 2 and modifier genes: an update on clinical and pathomolecular aspects.
P2860
Q39081415-F4B5FE82-572F-45C0-AD9A-1CC0FDC18711
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http://www.wikidata.org/entity/statement/Q39081415-F4B5FE82-572F-45C0-AD9A-1CC0FDC18711
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48aaae6ef87a344b862039af86f8baadad2270fa
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.