The muscular dystrophies

This publication has 62 references indexed in Scilit:

• An agrin minigene rescues dystrophic symptoms in a mouse model for congenital muscular dystrophy
  Nature, 2001
• In Vivoandin VitroCorrection of themdxDystrophin Gene Nonsense Mutation by Short-Fragment Homologous Replacement
  Human Gene Therapy, 2001
• LMNA, encoding lamin A/C, is mutated in partial lipodystrophy
  Nature Genetics, 2000
• Missense Mutations in the Rod Domain of the Lamin A/C Gene as Causes of Dilated Cardiomyopathy and Conduction-System Disease
  New England Journal of Medicine, 1999
• Dystrophin expression in the mdx mouse restored by stem cell transplantation
  Nature, 1999
• Skeletal muscle-specific expression of a utrophin transgene rescues utrophin-dystrophin deficient mice
  Nature Genetics, 1998
• Amelioration of the dystrophic phenotype of mdx mice using a truncated utrophin transgene
  Nature, 1996
• Population frequencies of inherited neuromuscular diseases—A world survey
  Neuromuscular Disorders, 1991
• PREDNISONE IN DUCHENNE MUSCULAR DYSTROPHY
  The Lancet, 1974
• Unusual type of benign x-linked muscular dystrophy.
  Journal of Neurology, Neurosurgery & Psychiatry, 1966