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Q33906048-0F7CCAB9-01B7-4BC1-860B-701DD0999D5C
Q33906048-0F7CCAB9-01B7-4BC1-860B-701DD0999D5C
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http://www.wikidata.org/entity/statement/Q33906048-0F7CCAB9-01B7-4BC1-860B-701DD0999D5C
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
Q33906048-0F7CCAB9-01B7-4BC1-860B-701DD0999D5C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33906048-0F7CCAB9-01B7-4BC1-860B-701DD0999D5C
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type
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wasDerivedFrom
2e3340473f83398c1105f019ba8bdbcd9d669912
P2860
Sensitive and quantitative universal Pyrosequencing methylation analysis of CpG sites