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Q54622558-6936D1FC-8B64-4B6F-8F4E-7195FE2C6BAA
Q54622558-6936D1FC-8B64-4B6F-8F4E-7195FE2C6BAA
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http://www.wikidata.org/entity/statement/Q54622558-6936D1FC-8B64-4B6F-8F4E-7195FE2C6BAA
Myotonia congenita and myotonic dystrophy in the same family: coexistence of a CLCN1 mutation and expansion in the CNBP (ZNF9) gene.
P2860
Q54622558-6936D1FC-8B64-4B6F-8F4E-7195FE2C6BAA
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http://www.wikidata.org/entity/statement/Q54622558-6936D1FC-8B64-4B6F-8F4E-7195FE2C6BAA
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321549a213bbb0fde8130c3637358f3c8cb05610
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.