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Q39012035-8444E4A0-9E6A-42D5-9E58-E1AFF7B104A2
Q39012035-8444E4A0-9E6A-42D5-9E58-E1AFF7B104A2
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http://www.wikidata.org/entity/statement/Q39012035-8444E4A0-9E6A-42D5-9E58-E1AFF7B104A2
Myotonic Dystrophy Type 2: An Update on Clinical Aspects, Genetic and Pathomolecular Mechanism.
P2860
Q39012035-8444E4A0-9E6A-42D5-9E58-E1AFF7B104A2
BestRank
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http://www.wikidata.org/entity/statement/Q39012035-8444E4A0-9E6A-42D5-9E58-E1AFF7B104A2
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d13cbf17f580e84e6f5d5bf4d06df23f8b256c8f
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.