DOI: 10.1055/s-00034916

Nervenheilkunde

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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