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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 (Molecular Vision, 2003)

Purpose: To determine if mutations in the retinal transcription factor gene NRL are associated with retinopathies other than autosomal dominant retinitis pigmentosa (adRP). Methods: Genomic DNA was isolated from blood ...