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378566
378566
http://dx.doi.org/10.1086/378566
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.
P356
Q33906048-F29C5FFA-59C0-41EE-8E6B-C3F78E612CAA
P356
378566
http://dx.doi.org/10.1086/378566