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Q36406299-BFDE950B-1E01-4542-BDE9-2F710E95B61D
Q36406299-BFDE950B-1E01-4542-BDE9-2F710E95B61D
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http://www.wikidata.org/entity/statement/Q36406299-BFDE950B-1E01-4542-BDE9-2F710E95B61D
Watson-Crick-like pairs in CCUG repeats: evidence for tautomeric shifts or protonation.
P2860
Q36406299-BFDE950B-1E01-4542-BDE9-2F710E95B61D
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http://www.wikidata.org/entity/statement/Q36406299-BFDE950B-1E01-4542-BDE9-2F710E95B61D
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00fd952414c72837e7201c30f67d8fd2ad7ed596
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.