1. Amorosi, B., Giustini, S., Rossi, A., et al. (1999). Myotonic dystrophy (Steinert disease): a morphologic and biochemical hair study. International Journal of Dermatology, 38, 434–438.
2. Bird TD (2007) Myotonic dystrophy type 1. GeneReviews. Updated November 15, 2007. Available at:
http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=myotonic-d
3. Brook, J. D., McCurrach, M. E., Genet, H. H., et al. (1992). Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member. Cell, 68, 799–808.
4. Bundley, S. (1982). Clinical evidence for heterogeneity in myotonic dystrophy. Journal of Medical Genetics, 19, 341–348.
5. Conravey, A., & Santana-Gould, L. (2010). Myotonia congenita and myotonic dystrophy surveillance and management. Current Treatment Options in Neurology, 12, 16–28.