Leptin and the metabolic syndrome in patients with myotonic dystrophy type 1
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0404.2009.01237.x/fullpdf
Reference24 articles.
1. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3â² end of a transcript encoding a protein kinase family member;Brook;Cell,1992
2. RNA metabolism in myotonic dystrophy;Morone;J Clin Invest,1997
3. Insulin receptor splicing alteration in myotonic dystrophy type 2;Savkur;Am J Hum Genet,2004
4. Dominant non-coding repeat expansions in human disease;Dick;Genome Dyn,2006
5. Abnormal release of incretins and cortisol after oral glucose in subjects with insulin-resistant myotonic dystrophy;Johansson;Eur J Endocrinol,2002
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