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Q34627289-D0756545-3FD3-4846-95CD-328DC7C6C60E
Q34627289-D0756545-3FD3-4846-95CD-328DC7C6C60E
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http://www.wikidata.org/entity/statement/Q34627289-D0756545-3FD3-4846-95CD-328DC7C6C60E
Population frequency of myotonic dystrophy: higher than expected frequency of myotonic dystrophy type 2 (DM2) mutation in Finland.
P2860
Q34627289-D0756545-3FD3-4846-95CD-328DC7C6C60E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34627289-D0756545-3FD3-4846-95CD-328DC7C6C60E
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663d524f2db754ab746bff671ae6e9e5ed74a7ce
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.