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Q33906048-115233D2-8AEC-4A43-9427-FBC057209142
Q33906048-115233D2-8AEC-4A43-9427-FBC057209142
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http://www.wikidata.org/entity/statement/Q33906048-115233D2-8AEC-4A43-9427-FBC057209142
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.
P31
Q33906048-115233D2-8AEC-4A43-9427-FBC057209142
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33906048-115233D2-8AEC-4A43-9427-FBC057209142
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wasDerivedFrom
d810c90d0fe9bc22012c57fc0927c096edcccb59
P31
scholarly article