Myotonic dystrophy type 1 (DM1): A triplet repeat expansion disorder
Author:
Publisher
Elsevier BV
Subject
Genetics,General Medicine
Reference44 articles.
1. Triplet-primed PCR is more sensitive than Southern blotting-long PCR for the diagnosis of myotonic dystrophy type1;Addis;Genet. Test. Mol. Biomarkers,2012
2. The CTG repeat expansion size correlates with the splicing defects observed in muscles from myotonic dystrophy type 1 patients;Botta;J. Med. Genet.,2008
3. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member;Brook;Cell,1992
4. Myotonic dystrophy kinase modulates skeletal muscle but not cardiac voltage-gated sodium channels;Chahine;FEBS Lett.,1997
5. MBNL1 and CUGBP1 modify expanded CUG-induced toxicity in a drosophila model of myotonic dystrophy 1;de Haro;Hum. Mol. Genet.,2006
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