Wu et al., 2016
- Haploinsufficiency of RCBTB1 is Associated with Coats Disease and Familial Exudative Vitreoretinopathy.
Human molecular genetics
25(8):1637-47
Full text @ Hum. Mol. Genet.
| Marker Type | Symbol | Name |
|---|---|---|
| Gene | ndp | norrin cystine knot growth factor NDP |
| Gene | rcbtb1 | regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 1 |
| Gene | tp53 | tumor protein p53 |