[Mutations in the HSN2 exon of WNK1 cause hereditary sensory neuropathy type II]

Med Sci (Paris). 2009 Mar;25(3):235-8. doi: 10.1051/medsci/2009253235.
[Article in French]
No abstract available

Publication types

  • News

MeSH terms

  • DNA Primers
  • Exons / genetics*
  • Female
  • Hereditary Sensory and Autonomic Neuropathies / genetics*
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • Male
  • Minor Histocompatibility Antigens
  • Mutation*
  • Nerve Tissue Proteins / genetics*
  • Polymorphism, Single Nucleotide*
  • Protein Serine-Threonine Kinases / genetics*
  • Reverse Transcriptase Polymerase Chain Reaction
  • WNK Lysine-Deficient Protein Kinase 1

Substances

  • DNA Primers
  • Intracellular Signaling Peptides and Proteins
  • Minor Histocompatibility Antigens
  • Nerve Tissue Proteins
  • Protein Serine-Threonine Kinases
  • WNK Lysine-Deficient Protein Kinase 1
  • WNK1 protein, human