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.
| Marker Type | Symbol | Name |
|---|---|---|
| Gene | ncapg2 | non-SMC condensin II complex, subunit G2 |
| Gene | nphp1 | nephronophthisis 1 |