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Q33906048-2B086F23-7EDF-43EE-9B0F-4ECC87C6AB6B
Q33906048-2B086F23-7EDF-43EE-9B0F-4ECC87C6AB6B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33906048-2B086F23-7EDF-43EE-9B0F-4ECC87C6AB6B
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.
P698
Q33906048-2B086F23-7EDF-43EE-9B0F-4ECC87C6AB6B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33906048-2B086F23-7EDF-43EE-9B0F-4ECC87C6AB6B
rank
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type
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Statement
wasDerivedFrom
d810c90d0fe9bc22012c57fc0927c096edcccb59
P698
12970845
http://www.w3.org/2001/XMLSchema#string