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., ...Daha Fazla

MOLECULAR VISION, cilt.9, ss.14-17, 2003 (SCI İndekslerine Giren Dergi) identifier identifier identifier

  • Cilt numarası: 9
  • Basım Tarihi: 2003
  • Dergi Adı: MOLECULAR VISION
  • Sayfa Sayıları: ss.14-17

Özet

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