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Q33906048-42B93E65-25AE-4C27-A864-E20F312DE158
Q33906048-42B93E65-25AE-4C27-A864-E20F312DE158
BestRank
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http://www.wikidata.org/entity/statement/Q33906048-42B93E65-25AE-4C27-A864-E20F312DE158
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.
P2860
Q33906048-42B93E65-25AE-4C27-A864-E20F312DE158
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33906048-42B93E65-25AE-4C27-A864-E20F312DE158
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type
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wasDerivedFrom
2e3340473f83398c1105f019ba8bdbcd9d669912
P2860
Sequential imputation for multilocus linkage analysis