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Q38852912-76245062-DA5C-41A5-959C-BCBD3B113FB7
Q38852912-76245062-DA5C-41A5-959C-BCBD3B113FB7
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http://www.wikidata.org/entity/statement/Q38852912-76245062-DA5C-41A5-959C-BCBD3B113FB7
Cultured myoblasts from patients affected by myotonic dystrophy type 2 exhibit senescence-related features: ultrastructural evidence.
P2860
Q38852912-76245062-DA5C-41A5-959C-BCBD3B113FB7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38852912-76245062-DA5C-41A5-959C-BCBD3B113FB7
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078857ecd5fd9cd528e83be89e7c88503f1b3157
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.