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Q33906048-AAB287DD-8595-4187-89D1-66B01BF5B70C
Q33906048-AAB287DD-8595-4187-89D1-66B01BF5B70C
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http://www.wikidata.org/entity/statement/Q33906048-AAB287DD-8595-4187-89D1-66B01BF5B70C
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.
P1433
Q33906048-AAB287DD-8595-4187-89D1-66B01BF5B70C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33906048-AAB287DD-8595-4187-89D1-66B01BF5B70C
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wasDerivedFrom
d810c90d0fe9bc22012c57fc0927c096edcccb59
P1433
American Journal of Human Genetics