QuickView for norbin (gene)

1. A postzygotic de novo NCDN mutation identified in a sporadic FTLD patient results in neurochondrin h…
2. Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability,…
3. Generation of a human Neurochondrin deficient iPSC line KICRi002-A-3 using CRISPR/Cas9.
4. Neurochondrin immunoglobulin G - Associated myelopathy - Ataxia syndrome.
5. FoxO3a negatively regulates nerve growth factor-induced neuronal differentiation through inhibiting …

There were no clinical trials for norbin