Author:
Suominen Tiina,Bachinski Linda L,Auvinen Satu,Hackman Peter,Baggerly Keith A,Angelini Corrado,Peltonen Leena,Krahe Ralf,Udd Bjarne
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference31 articles.
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4. Bachinski LL, Udd B, Meola G et al: 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. Am J Hum Genet 2003; 73: 835–848.
5. Liquori CL, Ricker K, Moseley ML et al: Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9. Science 2001; 293: 864–867.
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