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., ...Daha Fazla

MOLECULAR VISION, cilt.9, ss.14-17, 2003 (SCI-Expanded, Scopus)

Yayın Türü: Makale / Tam Makale
Cilt numarası: 9
Basım Tarihi: 2003
Dergi Adı: MOLECULAR VISION
Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
Sayfa Sayıları: ss.14-17
Hacettepe Üniversitesi Adresli: Hayır

Özet

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