Proximal myotonic myopathy syndrome in the absence of trinucleotide repeat expansions

Muscle Nerve. 1995 Jul;18(7):782-3. doi: 10.1002/mus.880180716.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • DNA Mutational Analysis
  • Diagnosis, Differential
  • Female
  • Humans
  • Male
  • Middle Aged
  • Myotonic Dystrophy / diagnosis*
  • Myotonic Dystrophy / genetics*
  • Myotonic Dystrophy / physiopathology
  • Repetitive Sequences, Nucleic Acid*