[A case of congenital myopathy with poor development of type I fibers, nuclear lesions and a focal myofibrillar involvement (author's transl)]

Arch Anat Cytol Pathol. 1976;24(4):275-9.
[Article in French]
No abstract available

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Cell Nucleus / ultrastructure
  • Female
  • Humans
  • Infant
  • Muscular Atrophy / congenital
  • Muscular Diseases / congenital*
  • Muscular Diseases / pathology
  • Myofibrils / ultrastructure
  • Syndrome