Article
CEP162 deficiency causes human retinal degeneration and reveals a dual role inciliogenesis…
medRxiv · 2022 · Nafisa Nuzhat
Key facts
| Title | CEP162 deficiency causes human retinal degeneration and reveals a dual role inciliogenesis and neurogenesis |
|---|---|
| First author | Nafisa Nuzhat |
| Journal | medRxiv |
| Published | May 20, 2022 |
| DOI | 10.1101/2021.11.23.469779 |
| Devices mentioned | K101223, K113129, K121993, K141068, K152205, K161194, K172649, K173648, K181444, K181594, K182569, K191194 and 27 more |
| Product codes mentioned | EPT, GCJ, GCT, GEX, HET, HJO, HLI, HLQ, HQF, KKX, OBO, QER and 8 more |
At a glance
- 10–99 FDA submissions mentioned
- 10–99 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