Myotonic Dystrophy: RNA Pathogenesis Comes into Focus
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics
Reference98 articles.
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3. 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;Bachinski;Am J Hum Genet,2003
4. Myotonia atrophica;Batten;Brain,1909
5. A novel homeodomain-encoding gene is associated with a large CpG island interrupted by the myotonic dystrophy unstable (CTG)n repeat;Boucher;Hum Mol Genet,1995
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