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Q33685609-C80BAED5-1E7D-466A-AB11-5FB500ADB4A3
Q33685609-C80BAED5-1E7D-466A-AB11-5FB500ADB4A3
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http://www.wikidata.org/entity/statement/Q33685609-C80BAED5-1E7D-466A-AB11-5FB500ADB4A3
Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population.
P2860
Q33685609-C80BAED5-1E7D-466A-AB11-5FB500ADB4A3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33685609-C80BAED5-1E7D-466A-AB11-5FB500ADB4A3
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5623e4d872b68b6726cdcb9f76d27e1c53970d81
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.