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Q33906048-1B3F3B44-1259-40BA-BC55-E0E395D7E171
Q33906048-1B3F3B44-1259-40BA-BC55-E0E395D7E171
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http://www.wikidata.org/entity/statement/Q33906048-1B3F3B44-1259-40BA-BC55-E0E395D7E171
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.
P2860
Q33906048-1B3F3B44-1259-40BA-BC55-E0E395D7E171
BestRank
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http://www.wikidata.org/entity/statement/Q33906048-1B3F3B44-1259-40BA-BC55-E0E395D7E171
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25a78406bd81105e7a0ab6143b76e322b3d05e66
P2860
Proximal myotonic dystrophy--a family with autosomal dominant muscular dystrophy, cataracts, hearing loss and hypogonadism: heterogeneity of proximal myotonic syndromes?