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; Sieving, P; Iannaccone, A; Musarella, M; Jacobson, S; Swaroop, A

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, Scopus)

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

Abstract

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