Mutation screening of patients with Leber congenital amaurosis or the enhanced S-cone syndrome reveals a lack of sequence variations in the NRL gene

Acar C., Mears A., Yashar B., Maheshwary A., Andreasson S., Baldi A., ...More

MOLECULAR VISION, vol.9, pp.14-17, 2003 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 9
  • Publication Date: 2003
  • Journal Name: MOLECULAR VISION
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.14-17
  • Hacettepe University Affiliated: No


Purpose: To determine if mutations in the retinal transcription factor gene NRL are associated with retinopathies other than autosomal dominant retinitis pigmentosa (adRP).