Novel mutations in the GRK1 gene in Japanese patients With Oguchi disease

Am J Ophthalmol. 2007 Sep;144(3):475-7. doi: 10.1016/j.ajo.2007.03.025.

Abstract

Purpose: To report novel mutations in the GRK1 gene in Japanese patients with Oguchi disease.

Design: Observational case report.

Methods: Two unrelated Japanese patients with Oguchi disease were examined. After informed consent was obtained, the coding regions of SAG and GRK1 were analyzed by direct sequencing.

Results: Although no mutation was found in SAG, two novel homozygous mutations in GRK1, c.1079 del T and c.1408-1412 CCCCC to CCC, were identified. Both mutations are expected to generate null alleles of GRK1.

Conclusions: The authors found two different novel mutations in Japanese patients. The results indicate that a considerable number of GRK1 mutations exist in the Japanese population.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Arrestin / genetics
  • Asian People
  • DNA Mutational Analysis
  • Electroretinography
  • Female
  • Frameshift Mutation*
  • G-Protein-Coupled Receptor Kinase 1 / genetics*
  • Humans
  • Intraocular Pressure
  • Night Blindness / genetics*
  • Polymerase Chain Reaction
  • Sequence Analysis, DNA
  • Visual Field Tests

Substances

  • Arrestin
  • G-Protein-Coupled Receptor Kinase 1
  • GRK1 protein, human