[Neurotrypsin mutations and mental retardation]

Med Sci (Paris). 2003 May;19(5):525-7. doi: 10.1051/medsci/2003195525.
[Article in French]
No abstract available

Publication types

  • News
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amyloid beta-Protein Precursor
  • Animals
  • Carrier Proteins / genetics
  • Central Nervous System / embryology
  • Codon, Nonsense
  • Humans
  • Intellectual Disability / genetics*
  • Kallikreins / deficiency
  • Kallikreins / genetics
  • Mice
  • Nerve Tissue Proteins / physiology
  • Protease Nexins
  • Rats
  • Receptors, Cell Surface
  • Sequence Deletion
  • Serine Endopeptidases / deficiency
  • Serine Endopeptidases / genetics*
  • Serine Endopeptidases / physiology
  • Synapses / chemistry
  • Synapses / physiology

Substances

  • Amyloid beta-Protein Precursor
  • Carrier Proteins
  • Codon, Nonsense
  • Nerve Tissue Proteins
  • Protease Nexins
  • Receptors, Cell Surface
  • KLK8 protein, human
  • Kallikreins
  • Serine Endopeptidases
  • neurotrypsin