ArticleAmerican journal of human genetics2003

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.

Linda L Bachinski et al.PubMed ↗Full text ↗Publisher ↗

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