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.
Target | Reagent |
---|---|
ncapg2 | MO1-ncapg2 |
nphp1 | MO3-nphp1 |