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Q38179289-303B0EDE-7D73-4938-83F2-3825611046E1
Q38179289-303B0EDE-7D73-4938-83F2-3825611046E1
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http://www.wikidata.org/entity/statement/Q38179289-303B0EDE-7D73-4938-83F2-3825611046E1
Recent advances in myotonic dystrophy type 2.
P2860
Q38179289-303B0EDE-7D73-4938-83F2-3825611046E1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38179289-303B0EDE-7D73-4938-83F2-3825611046E1
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2e6e97bcfa16fcc5d3a4e755385278e466e3bc70
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.