Gene for hereditary neuropathy with liability to pressure palsies (HNPP) maps to chromosome 17 at or close to the locus for HMSN type 1

This publication has 26 references indexed in Scilit:

• A Comprehensive Genetic Linkage Map of the Human Genome
  Science, 1992
• Improving the polymorphism content of the 3′ UTR of the human IGF2R gene
  Human Molecular Genetics, 1992
• The peripheral myelin protein gene PMP–22 is contained within the Charcot–Marie–Tooth disease type 1A duplication
  Nature Genetics, 1992
• The gene for the peripheral myelin protein PMP–22 is a candidate for Charcot–Marie–Tooth disease type 1A
  Nature Genetics, 1992
• The peripheral myelin gene PMP–22/GAS–3 is duplicated in Charcot–Marie–Tooth disease type 1A
  Nature Genetics, 1992
• Hereditary Neuropathy with Liability to Pressure Palsies in Childhood*
  Neuropediatrics, 1992
• Trembler mouse carries a point mutation in a myelin gene
  Nature, 1992
• Clinical and electrodiagnostic findings, nerve biopsy and blood group markers in a family with hereditary neuropathy with liability to pressure palsies
  Acta Neurologica Scandinavica, 1991
• A family with tomaculous neuropathy mimicking Charcot-Marie-Tooth disease
  Clinical Neurology and Neurosurgery, 1990
• Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17
  Experimental Neurology, 1989