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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| Description | scientific article |
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author: Mark D. Shriver Karin Jurkat-Rott Maija Wessman Josep Gamez Giovanni Meola |
| Publication date | September 10, 2003 |
| Language | English |
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