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Mutation and association analysis of the DAP-1 gene with schizophrenia.

Abstract
Glutamate dysfunction has been hypothesized to be involved in the pathophysiology of schizophrenia. The human homolog of Drosophila discs large protein (hDLG) and post-synaptic density-95-associated protein-1 (DAP-1) is one of the major proteins that are involved in intracellular signal transduction via N-methyl-d-aspartate receptors. In the present study 33 Japanese patients with schizophrenia were screened for mutations in the DAP-1 gene. A single nucleotide polymorphism was identified in the DAP-1 gene (1618A/G). A case-control study using a larger sample of unrelated patients and controls did not reveal a significant association between this polymorphism and schizophrenia. The results do not provide evidence that the DAP-1 gene is involved in vulnerability to schizophrenia.
AuthorsShinsuke Aoyama, Osamu Shirakawa, Hisae Ono, Takeshi Hashimoto, Yasuo Kajimoto, Kiyoshi Maeda
JournalPsychiatry and clinical neurosciences (Psychiatry Clin Neurosci) Vol. 57 Issue 5 Pg. 545-7 (Oct 2003) ISSN: 1323-1316 [Print] Australia
PMID12950712 (Publication Type: Journal Article)
Chemical References
  • DLGAP1 protein, human
  • Nerve Tissue Proteins
  • SAP90-PSD95 Associated Proteins
  • DNA
Topics
  • Case-Control Studies
  • DNA (genetics)
  • DNA Mutational Analysis
  • Female
  • Gene Frequency
  • Genotype
  • Humans
  • Male
  • Middle Aged
  • Mutation
  • Nerve Tissue Proteins (genetics)
  • Polymerase Chain Reaction
  • Polymorphism, Single-Stranded Conformational
  • SAP90-PSD95 Associated Proteins
  • Schizophrenia (genetics)

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