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.
Target | Reagent |
---|---|
ndp | MO1-ndp |
rcbtb1 | MO1-rcbtb1 |
MO2-rcbtb1 |