QuickView for NCDN;jsessionid=4FCDAD71E10E9874EA13FC17D3B67133 (gene)

1. A postzygotic de novo NCDN mutation identified in a sporadic FTLD patient results in neurochondrin h…
2. Generation of a human Neurochondrin deficient iPSC line KICRi002-A-3 using CRISPR/Cas9.
3. Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability,…
4. Neurochondrin immunoglobulin G - Associated myelopathy - Ataxia syndrome.
5. Operant training for highly palatable food alters translating mRNA in nucleus accumbens D2 neurons a…

There were no clinical trials for NCDN;jsessionid=4FCDAD71E10E9874EA13FC17D3B67133