Novel mutations in the connexin 32 gene associated with X-linked Charcot-Marie tooth disease

This publication has 22 references indexed in Scilit:

• Mutations in the connexin 32 gene in X-linked dominant Charcot- Marie - Tooth disease (CMTX1)
  Human Molecular Genetics, 1994
• Connexin Mutations in X-Linked Charcot-Marie-Tooth Disease
  Science, 1993
• Mutation of the myelin Po gene in Charcot — Marie — Tooth neuropathy type 1B
  Human Molecular Genetics, 1993
• Deletion of the serine 34 codon from the major peripheral myelin protein P0 gene in Charcot–Marie–Tooth disease type 1B
  Nature Genetics, 1993
• Charcot–Marie–Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene
  Nature Genetics, 1993
• X-LINKED DOMINANT HEREDITARY MOTOR AND SENSORY NEUROPATHY
  Brain, 1990
• Molecular characterization and functional expression of the human cardiac gap junction channel.
  The Journal of cell biology, 1990
• Connexin43: a protein from rat heart homologous to a gap junction protein from liver.
  The Journal of cell biology, 1987
• Identification of a rat liver cDNA and mRNA coding for the 28 kDa gap junction protein
  FEBS Letters, 1986
• Cloning and characterization of human and rat liver cDNAs coding for a gap junction protein.
  The Journal of cell biology, 1986