Khan et al., 2019
- Mutations in NCAPG2 Cause a Severe Neurodevelopmental Syndrome that Expands the Phenotypic Spectrum of Condensinopathies.
American journal of human genetics
104:94-111
Full text @ Am. J. Hum. Genet.
| Human Disease | Fish | Environment | Evidence Code |
|---|---|---|---|
| autosomal recessive disease |
WT + MO1-ncapg2 WT + CRISPR1-ncapg2 WT + CRISPR2-ncapg2 |
standard conditions standard conditions standard conditions |
|