Article Versions Notes

Stingl K, Baumann B, De Angeli P, Vincent A, Héon E, Cordonnier M, De Baere E, Raskin S, Sato MT, Shiokawa N, et al. Novel OPN1LW/OPN1MW Exon 3 Haplotype-Associated Splicing Defect in Patients with X-Linked Cone Dysfunction. International Journal of Molecular Sciences. 2022; 23(12):6868. https://doi.org/10.3390/ijms23126868

Stingl, Katarina, Britta Baumann, Pietro De Angeli, Ajoy Vincent, Elise Héon, Monique Cordonnier, Elfriede De Baere, Salmo Raskin, Mario Teruo Sato, Naoye Shiokawa, and et al. 2022. "Novel OPN1LW/OPN1MW Exon 3 Haplotype-Associated Splicing Defect in Patients with X-Linked Cone Dysfunction" International Journal of Molecular Sciences 23, no. 12: 6868. https://doi.org/10.3390/ijms23126868

Stingl, K., Baumann, B., De Angeli, P., Vincent, A., Héon, E., Cordonnier, M., De Baere, E., Raskin, S., Sato, M. T., Shiokawa, N., Kohl, S., & Wissinger, B. (2022). Novel OPN1LW/OPN1MW Exon 3 Haplotype-Associated Splicing Defect in Patients with X-Linked Cone Dysfunction. International Journal of Molecular Sciences, 23(12), 6868. https://doi.org/10.3390/ijms23126868