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Q38093802-8EFF3D9C-98D3-4F67-B78D-45A14693B5FA
Q38093802-8EFF3D9C-98D3-4F67-B78D-45A14693B5FA
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Statement
http://www.wikidata.org/entity/statement/Q38093802-8EFF3D9C-98D3-4F67-B78D-45A14693B5FA
The diagnosis and treatment of myotonic disorders.
P2860
Q38093802-8EFF3D9C-98D3-4F67-B78D-45A14693B5FA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38093802-8EFF3D9C-98D3-4F67-B78D-45A14693B5FA
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wasDerivedFrom
3c9e6e032de40806640e0e78e035175b0bc9d538
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.