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.
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F. Wright | M. Shriver | R. Moxley | G. Meola | P. Harper | G. Bassez | F. Lehmann-Horn | K. Jurkat-Rott | B. Eymard | M. Wessman | R. Krahe | C. Thornton | M. Rogers | A. Bottani | R. Sallinen | L. Bachinski | B. Udd | V. Sansone | J. Gámez | T. Wieser | Shanxiang Zhang | C. Navarro | A. Kohler