DOI:
10.1055/s-00034916
Nervenheilkunde
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References
Bachinski LL, Udd B, Meola G, Sansone V, Bassez G, Eymard B. 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: 835-48.
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