41st ENMC international workshop on congenital muscular dystrophy 8–10 March 1996, Naarden, The Netherlands

This publication has 22 references indexed in Scilit:

• Merosin-negative congenital muscular dystrophy, occipital epilepsy with periodic spasms and focal cortical dysplasia. Report of three Italian cases in two families
  Brain & Development, 1996
• Domains of laminin
  Journal of Cellular Biochemistry, 1996
• Congenital muscular dystrophy and severe central nervous system atrophy in two siblings
  Acta Neuropathologica, 1995
• Merosin‐negative congenital muscular dystrophy associated with extensive brain abnormalities
  Neurology, 1995
• Mutations in the laminin α2–chain gene (LAMA2) cause merosin–deficient congenital muscular dystrophy
  Nature Genetics, 1995
• Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal
  Neuromuscular Disorders, 1995
• Prenatal diagnosis in congenital muscular dystrophy
  The Lancet, 1995
• Murine muscular dystrophy caused by a mutation in the laminin α2 (Lama2) gene
  Nature Genetics, 1994
• A new nomenclature for the laminins
  Matrix Biology, 1994
• Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31–33
  Nature Genetics, 1993