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Q38209927-461F744A-80EB-4AF6-8009-32D66441605D
Q38209927-461F744A-80EB-4AF6-8009-32D66441605D
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http://www.wikidata.org/entity/statement/Q38209927-461F744A-80EB-4AF6-8009-32D66441605D
Clinical aspects, molecular pathomechanisms and management of myotonic dystrophies.
P2860
Q38209927-461F744A-80EB-4AF6-8009-32D66441605D
BestRank
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http://www.wikidata.org/entity/statement/Q38209927-461F744A-80EB-4AF6-8009-32D66441605D
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ea37b40e38639e8556d6873ebd23c2436b4cc29b
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.