Report of the 83rd ENMC International Workshop: 4th Workshop on Nemaline Myopathy, 22–24 September 2000, Naarden, The Netherlands

This publication has 10 references indexed in Scilit:

• Abnormalities in the expression of nebulin in chromosome-2 linked nemaline myopathy
  Neuromuscular Disorders, 2001
• Nebulin expression in patients with nemaline myopathy
  Neuromuscular Disorders, 2001
• Myozenin: An alpha -actinin- and gamma -filamin-binding protein of skeletal muscle Z lines
  Proceedings of the National Academy of Sciences, 2001
• A mutation in alpha-tropomyosinslow affects muscle strength, maturation and hypertrophy in a mouse model for nemaline myopathy
  Human Molecular Genetics, 2001
• An autosomal dominant congenital myopathy with cores and rods is associated with a neomutation in the RYR1 gene encoding the skeletal muscle ryanodine receptor
  Human Molecular Genetics, 2000
• A Novel Nemaline Myopathy in the Amish Caused by a Mutation in Troponin T1
  American Journal of Human Genetics, 2000
• Myotilin is mutated in limb girdle muscular dystrophy 1A
  Human Molecular Genetics, 2000
• Report of the 70th ENMC International Workshop: Nemaline myopathy, 11–13 June 1999, Naarden, The Netherlands
  Neuromuscular Disorders, 2000
• Sequencing, Expression Analysis, and Mapping of Three Unique Human Tropomodulin Genes and Their Mouse Orthologs
  Genomics, 2000
• Mutations in the skeletal muscle α-actin gene in patients with actin myopathy and nemaline myopathy
  Nature Genetics, 1999