Novel OPN1LW/OPN1MW Exon 3 Haplotype-Associated Splicing Defect in Patients with X-Linked Cone Dysfunction

Stingl, K; Baumann, B; De Angeli, P; Vincent, A; Heon, E; Cordonnier, M; De Baere, E; Raskin, S; Sato, MT; Shiokawa, N; Kohl, S; Wissinger, B

Wissinger, B (通讯作者),Univ Tubingen, Ctr Ophthalmol, Inst Ophthalm Res, D-72076 Tubingen, Germany.

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022; 23 (12):

Abstract

Certain combinations of common variants in exon 3 of OPN1LW and OPN1MW, the genes encoding the apo-protein of the long- and middle-wavelength sensitiv......

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