Charcot–Marie–Tooth neuropathy: clinical phenotypes of four novel mutations in the MPZ and Cx 32 genes

This publication has 32 references indexed in Scilit:

• Charcot–Marie–Tooth disease type 1
  Brain, 2000
• Molecular genetics and biology of inherited peripheral neuropathies: a fast-moving field
  neurogenetics, 1999
• Mutations in the peripheral myelin genes and associated genes in inherited peripheral neuropathies
  Human Mutation, 1999
• Connexin32 and X-linked Charcot–Marie–Tooth Disease
  Neurobiology of Disease, 1997
• Myelin protein zero (MPZ) gene mutations in nonduplication type 1 Charcot-Marie-Tooth disease
  Human Mutation, 1996
• Connexin Mutations in X-Linked Charcot-Marie-Tooth Disease
  Science, 1993
• Charcot-Marie-Tooth Disease Type 1A -- Association with a Spontaneous Point Mutation in the PMP22 Gene
  New England Journal of Medicine, 1993
• Conduction block in clinical practice
  Muscle & Nerve, 1991
• DNA duplication associated with Charcot-Marie-Tooth disease type 1A
  Cell, 1991
• Research criteria for diagnosis of chronic inflammatory demyelinating polyneuropathy (CIDP)
  Neurology, 1991