Expression of laminin subunits in congenital muscular dystrophy

This publication has 20 references indexed in Scilit:

• Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal
  Neuromuscular Disorders, 1995
• Somatosensory and Visual Evoked Potentials in Congenital Muscular Dystrophy: Correlation with MRI Changes and Muscle Merosin Status
  Neuropediatrics, 1995
• Expression of novel 400‐kDa laminin chains by mouse and bovine endothelial cells
  European Journal of Biochemistry, 1994
• Human laminin M chain (merosin): complete primary structure, chromosomal assignment, and expression of the M and A chain in human fetal tissues
  The Journal of cell biology, 1994
• Dystrophin–glycoprotein complex: Its role in the molecular pathogenesis of muscular dystrophies
  Muscle & Nerve, 1994
• Deficiency of dystrophin-associated proteins: A common mechanism leading to muscle cell necrosis in severe childhood muscular dystrophies
  Neuromuscular Disorders, 1993
• Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31–33
  Nature Genetics, 1993
• Abnormal expression of dystrophin-associated proteins in Fukuyama-type congenital muscular dystrophy
  The Lancet, 1993
• Myosin isoforms in congenital muscular dystrophy
  Pediatric Neurology, 1992
• Genetically determined defect of Schwann cell basement membrane in dystrophic mouse
  Nature, 1975