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, T. D. (2013). Myotonic dystrophy type 1. GeneReviews. Updated 16 May 2013. Available at:
http://www.ncbi.nlm.nih.gov/books/NBK1165/
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. Conravey, A., & Santana-Gould, L. (2010). Myotonia congenita and myotonic dystrophy surveillance and management. Current Treatment Options in Neurology, 12, 16–28.
5. Dalton, J. C., Ranum, L. P. W., & Day, J. W. (2013). Myotonic dystrophy type 2. GeneReviews. Updated 3 July 2013. Available at:
http://www.ncbi.nlm.nih.gov/books/NBK1466/