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Q33906048-0AD4B1EA-3457-446A-9203-323C49F0BEA3
Q33906048-0AD4B1EA-3457-446A-9203-323C49F0BEA3
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http://www.wikidata.org/entity/statement/Q33906048-0AD4B1EA-3457-446A-9203-323C49F0BEA3
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
Q33906048-0AD4B1EA-3457-446A-9203-323C49F0BEA3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33906048-0AD4B1EA-3457-446A-9203-323C49F0BEA3
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type
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wasDerivedFrom
25a78406bd81105e7a0ab6143b76e322b3d05e66
P2860
Faster linkage analysis computations for pedigrees with loops or unused alleles.