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Q36979268-931F67DF-CB9C-4445-B71A-F4F8338434F3
Q36979268-931F67DF-CB9C-4445-B71A-F4F8338434F3
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http://www.wikidata.org/entity/statement/Q36979268-931F67DF-CB9C-4445-B71A-F4F8338434F3
Myotonic dystrophy type 2 found in two of sixty-three persons diagnosed as having fibromyalgia.
P2860
Q36979268-931F67DF-CB9C-4445-B71A-F4F8338434F3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36979268-931F67DF-CB9C-4445-B71A-F4F8338434F3
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wasDerivedFrom
c6c9ac63981c6c16281bfd07bed1496eaffd637c
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.