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Q37180513-AF863D3B-811B-433D-97F7-1B7592270FF1
Q37180513-AF863D3B-811B-433D-97F7-1B7592270FF1
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http://www.wikidata.org/entity/statement/Q37180513-AF863D3B-811B-433D-97F7-1B7592270FF1
Premutation allele pool in myotonic dystrophy type 2.
P2860
Q37180513-AF863D3B-811B-433D-97F7-1B7592270FF1
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Statement
http://www.wikidata.org/entity/statement/Q37180513-AF863D3B-811B-433D-97F7-1B7592270FF1
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241fd7cadae9af656f05ac5f7e245438b814a2a4
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.