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Q35738537-D7B86289-E03F-411B-A027-5C4280BCBBD3
Q35738537-D7B86289-E03F-411B-A027-5C4280BCBBD3
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http://www.wikidata.org/entity/statement/Q35738537-D7B86289-E03F-411B-A027-5C4280BCBBD3
Myotonic dystrophy: RNA pathogenesis comes into focus.
P2860
Q35738537-D7B86289-E03F-411B-A027-5C4280BCBBD3
BestRank
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http://www.wikidata.org/entity/statement/Q35738537-D7B86289-E03F-411B-A027-5C4280BCBBD3
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b3bd85593737c19ecfdb3f38939739f041575f23
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.