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Q33906048-E8710D43-DDF4-4A9F-9321-718AD188B841
Q33906048-E8710D43-DDF4-4A9F-9321-718AD188B841
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33906048-E8710D43-DDF4-4A9F-9321-718AD188B841
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.
P407
Q33906048-E8710D43-DDF4-4A9F-9321-718AD188B841
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33906048-E8710D43-DDF4-4A9F-9321-718AD188B841
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P407
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