LabCAST

Diagnosis and Management of Myotonic Dystrophy
SessionReferences
  1. Adams, C. Myotonic Dystrophy Review in GeneReviews at GeneTests·GeneClinics: Medical Genetics Information Resource [online database] 2001. University of Washington, Seattle. http://www.geneclinics.org
  2. Liquori, C.L., et al., Myotonic Dystrophy Type 2 Caused by a CCTG Expansion in Intron 1 of ZNF9. Science 2001; 293:864-867.
  3. "Facts about Myotonic Muscular Dystrophy." Muscular Dystrophy Association, Tucson, 2000.
  4. Webb, D. et al., Myotonia Dystrophica: Obstetric Complications. American Journal of Obstetrics and Gynecology 1978; 132:265-70.
  5. Mathieu, J. et al., A 10-year Study of Mortality in a Cohort of Patients with Myotonic Dystrophy. Neurology 1999; 52:1658-1662.
  6. Die-Smulders, C.E. et al., Age and Causes of Death in Adult-onset Myotonic Dystrophy. Brain 1998; 121 (Pt 8):1557-1563.
  7. Redman, J.B. et al., Relationship Between Parental Trinucleotide CTG Repeat Length and Severity of Myotonic Dystrophy in Offspring. JAMA 1993; 269:1960-1965.
  8. Philips, A.V. et al., Disruption of Splicing Regulated by a CUG-binding Protein in Myotonic Dystrophy. Science 1998; 280:696-697.
  9. Roses, A.D., Chang, L. Myotonic Dystrophy. MedLink Neurology Clinical Studies 2002. http://www.medlink.com
  10. Harper, P.S. et al., Myotonic Dystrophy. In Myology, Basic and Clinical, Second Edition, ed. Engel, AG et al., 1208. 1994. New York: McGraw-Hill, Inc.
  11. Nelson, W.E. et al., Myotonic muscular dystrophy in Textbook of pediatrics, 15th edition, 1749-1750. 1996. Philadelphia: WB Saunders Co.