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

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

Author: Stingl, Katarina; Baumann, Britta; De Angeli, Pietro; Vincent, Ajoy; Heon, Elise; Cordonnier, Monique; De Baere, Elfriede; Raskin, Salmo; Sato, Mario Teruo; Shiokawa, Naoye; Kohl, Susanne; Wissinger, Bernd
Tübinger Autor(en):
Baumann, Britta
De Angeli, Pietro
Kohl, Susanne
Wissinger, Bernd
Štingl, Katarína
Published in: International Journal of Molecular Sciences (2022), Bd. 23 (12), Article 6868
Verlagsangabe: Mdpi
Language: English
Full text: http://dx.doi.org/10.3390/ijms23126868
ISSN: 1422-0067
DDC Classifikation: 540 - Chemistry and allied sciences
570 - Life sciences; biology
Dokumentart: Article
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