Article
The Okur-Chung Neurodevelopmental Syndrome (OCNDS) mutation CK2K198R leads to a rewiring…
medRxiv · 2021 · Caefer, D. M.; Phan, N. Q.; Liddle, J. C.; Balsbaugh, J. L.; O'Shea, J. P.; Tzingounis, A. V.; Schwartz, D.
Key facts
| Title | The Okur-Chung Neurodevelopmental Syndrome (OCNDS) mutation CK2K198R leads to a rewiring of kinase specificity |
|---|---|
| First author | Caefer, D. M.; Phan, N. Q.; Liddle, J. C.; Balsbaugh, J. L.; O'Shea, J. P.; Tzingounis, A. V.; Schwartz, D. |
| Journal | medRxiv |
| Published | Apr 5, 2021 |
| DOI | 10.1101/2021.04.05.438522 |
| Devices mentioned | K103302 |
| Product codes mentioned | NDS, NJT, OOI |
At a glance
- 1–9 FDA submissions mentioned
- 1–9 Product codes mentioned
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