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, CEREN; 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

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Acar C., MEARS A., YASHAR B., MAHESHWARY A., ANDREASSON S., BALDI A., ...More

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

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
Inonu 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).