Article
Missense mutations in CRX homeodomain cause dominant retinopathies through two distinct…
eLife · 2023 · Yiqiao Zheng, author Chi Sun, author Xiaodong Zhang, author Philip A Ruzycki, author Shiming Chen, author ([email protected]) Paschalis Kratsios, editor Claude Desplan, senior_editor
Key facts
| Title | Missense mutations in CRX homeodomain cause dominant retinopathies through two distinct mechanisms |
|---|---|
| First author | Yiqiao Zheng, author Chi Sun, author Xiaodong Zhang, author Philip A Ruzycki, author Shiming Chen, author ([email protected]) Paschalis Kratsios, editor Claude Desplan, senior_editor |
| Journal | eLife |
| Published | Nov 14, 2023 |
| DOI | 10.7554/eLife.87147.4 |
| Devices mentioned | K042152, K042268, K810863, K940422, K982100 |
| Product codes mentioned | CFN, DBM, DFZ, MQP, NSU, PFF, PFT |
At a glance
- 1–9 FDA submissions mentioned
- 1–9 Product codes mentioned
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About Literature
Peer-reviewed and preprint literature indexed by Orca1 and linked to the FDA submissions and product codes each article mentions. Only bibliographic details are shown here.
Source: Publisher and PubMed metadata; device mentions identified by Orca1